Label: Allergenic Extract
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Contains inactivated NDC Code(s)
NDC Code(s): 36987-1197-1, 36987-1197-2, 36987-1197-3, 36987-1197-4, view more36987-1201-1, 36987-1201-2, 36987-1201-3, 36987-1201-4, 36987-1205-1, 36987-1205-2, 36987-1205-3, 36987-1205-4, 36987-1209-1, 36987-1209-2, 36987-1209-3, 36987-1209-4, 36987-1213-1, 36987-1213-2, 36987-1213-3, 36987-1213-4, 36987-1217-1, 36987-1217-2, 36987-1217-3, 36987-1217-4, 36987-1221-1, 36987-1221-2, 36987-1221-3, 36987-1221-4, 36987-1225-1, 36987-1225-2, 36987-1225-3, 36987-1225-4, 36987-1229-1, 36987-1229-2, 36987-1229-3, 36987-1229-4, 36987-1233-1, 36987-1233-2, 36987-1233-3, 36987-1233-4, 36987-1237-1, 36987-1237-2, 36987-1237-3, 36987-1237-4, 36987-1241-1, 36987-1241-2, 36987-1241-3, 36987-1241-4, 36987-1245-1, 36987-1245-2, 36987-1245-3, 36987-1245-4, 36987-1249-1, 36987-1249-2, 36987-1249-3, 36987-1249-4, 36987-1253-1, 36987-1253-2, 36987-1253-3, 36987-1253-4, 36987-1257-1, 36987-1257-2, 36987-1257-3, 36987-1257-4, 36987-1261-1, 36987-1261-2, 36987-1261-3, 36987-1261-4, 36987-1265-1, 36987-1265-2, 36987-1265-3, 36987-1265-4, 36987-1269-1, 36987-1269-2, 36987-1269-3, 36987-1269-4, 36987-1273-1, 36987-1273-2, 36987-1273-3, 36987-1273-4, 36987-1277-1, 36987-1277-2, 36987-1277-3, 36987-1277-4, 36987-1281-1, 36987-1281-2, 36987-1281-3, 36987-1281-4 - Packager: Nelco Laboratories, Inc.
- Category: HUMAN PRESCRIPTION DRUG LABEL
- DEA Schedule: None
- Marketing Status: Biologic Licensing Application
Drug Label Information
Updated December 10, 2009
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BOXED WARNING
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WARNING
Diagnostic and therapeutic allergenic extracts are intended to be administered by a physician who is an allergy specialist and experienced in allergenic diagnostic testing and immunotherapy and the emergency care of anaphylaxis.
This product should not be injected intravenously. Deep subcutaneous routes have been safe. Sensitive patients may experience severe anaphylactic reactions resulting in respiratory obstruction, shock, coma and/or death. (See Adverse Reactions)
Serious adverse reactions should be reported to Nelco Laboratories immediately and a report filed to: MedWatch, The FDA Medical Product Problem Reporting Program, at 5600 Fishers Lane, Rockville, Md. 20852-9787, call 1-800-FDA-1088.
Extreme caution should be taken when using allergenic extracts for patients who are taking beta-blocker medications. In the event of a serious adverse reaction associated with the use of allergenic extracts, patients receiving beta-blockers may not be responsive to epinephrine or inhaled brochodialators.(1)(See Precautions)
Allergenic extracts should be used with caution for patients with unstable or steroid-dependent asthma or underlying cardiovascular disease. (See Contraindications)
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DESCRIPTION
Allergenic extracts are sterile solutions consisting of the extractable components from various biological sources including pollens, inhalants, molds, animal epidermals and insects. Aqueous extracts are prepared using cocas fluid containing NaCl 0.5%, NaHCO3 0.0275%, WFI, preservative 0.4% Phenol. Glycerinated allergenic extracts are prepared with cocas fluid and glycerin to produce a 50% (v/v) allergenic extract. Allergenic Extracts are supplied as concentrations designated as protein nitrogen units (PNU) or weight/volume (w/v) ratio. Standardized extracts are designated in Bioequivalent Allergy Units (BAU) or Allergy Units (AU). (See product insert for standardized extracts)
For diagnostic purposes, allergenic extracts are to be administered by prick-puncture or intradermal routes. Allergenic extracts are administered subcutaneously for immunotherapy injections.
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CLINICAL PHARMACOLOGY
The pharmacological action of allergenic extracts used diagnostically is based on the liberation of histamine and other substances when the allergen reacts with IgE antibodies attached to the mast cells. When allergenic extracts are used for immunotherapy, the effect is an increase in immunoglobulin G (IgG) and an increased T suppresser lymphocyte which interferes with the allergic response.(2) With repeated administration of allergenic extracts changes develop in regards to IgG and IgE production and mediator-releasing cells. The histamine release response is reduced in some patients.
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INDICATIONS AND USAGE
Allergenic extracts are indicated for use in diagnostic testing and as part of a treatment regime for allergic disease, as established by allergy history and skin test reactivity.
Allergenic extracts are indicated for the treatment of allergen specific allergic disease for use as hyposensitization or immunotherapy when avoidance of specific allergens can not be attained. The use of allergenic extracts for therapeutic purpose has been established by well-controlled clinical studies. Allergenic extracts may be used as adjunctive therapy along with pharmacotherapy which includes antihistamines, corticosteroids, and cromoglycate, and avoidance measures. Allergenic extracts for therapeutic use should be given using only the allergen selection to which the patient is allergic, has a history of exposure and are likely to be exposed to again.
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CONTRAINDICATIONS
Allergenic extracts should not be used if the patient has asthma, cardiovascular disease, emphysema, diabetes, bleeding diathesis or pregnancy, unless a specific diagnosis of type 1 allergic disease is made based on skin testing and the benefits of treatment outweigh the risks of an adverse reaction during testing or treatment. Allergenic extracts are not indicated for use in patients who are not clinically allergic or who are not skin reactive to an allergen. Allergenic extracts should be discontinued or the concentration of potency substantially reduced in patients who experience unacceptable adverse reactions.
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WARNINGS
Epinephrine 1:1000 should be available.
Concentrated extracts must be diluted with sterile diluent prior to first use on a patient for treatment or intradermal testing. All concentrates of glycerinated allergenic extracts have the ability to cause serious local and systemic reactions including death in sensitive patients. Sensitive patients may experience severe anaphylactic reactions resulting in respiratory obstruction, shock, coma and /or death.(4)(See Adverse Reactions) An allergenic extract should be temporarily withheld from patients or the dose of the extract adjusted downward if any of the following conditions exist: (1) Severe symptoms of rhinitis and/or asthma (2) Infections or flu accompanied by fever and (3) Exposure to excessive amounts of clinically relevant allergen prior to a scheduled injection. When switching patients to a new lot of the same extract the initial dose should be reduced 3/4 so that 25% of previous dose is administered.
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PRECAUTIONS
GENERAL: Epinephrine 1:1000 should be available as well as personnel trained in administering emergency treatment. Allergenic Extracts are not intended for intravenous injections. For safe and effective use of allergenic extracts, sterile diluents, sterile vials, sterile syringes should be used and aseptic precautions observed when making a dilution and/or administering the allergenic extract injection. A sterile tuberculin syringe graduated in 0.1 ml units to measure each dose for the prescribed dilution should be used. To reduce the risk of an occurrence of adverse reactions, begin with a careful personal history plus a physical exam. Confirm your findings with scratch or intradermal skin testing.
Standardized extracts are those labeled in AU/ml units or BAU/ml units. Standardized extracts are not interchangeable with extracts previously labeled as wt/vol or PNU/ml. Before administering a standardized extract, read the accompanying insert contained with standardized extracts.
Information for Patients: All concentrates of allergenic extracts have the ability to cause serious local and systemic reactions including death in sensitive patients. Patients should be informed of this risk prior to skin testing and immunotherapy. Patients should be instructed to recognize adverse reaction symptoms that may occur and to report all adverse reactions to a physician. Patients should be instructed to remain in the office for 30 minutes during testing using allergenic extracts and at least 30 minutes after therapeutic injections using allergenic extracts.
DRUG INTERACTIONS: Some drugs may affect the reactivity of the skin; patients should be instructed to avoid medications, particularly antihistamines and sympathomimetic drugs, for at least 24 hours prior to skin testing. Antihistamines and Hydroxyzine can significantly inhibit the immediate skin test reactions as they tend to neutralize or antagonize the action of histamine.(3) This effect has been primarily documented when testing was performed within 1 to 2 hours after drug ingestion. Partial inhibition of the skin test reaction had been observed for longer periods. Epinephrine injection inhibits the immediate skin test reactions for several hours. Patients on delayed absorption antihistamine tablets should be free of such medication for 48 hours before testing. Patients using Astemizole (Hismanal) may experience prolonged suppression and should be free from such medication for up to 6 to 8 weeks prior to testing. Refer to package insert from an applicable long acting antihistamine manufacturer for additional information.
Extreme caution should be taken when using allergenic extracts on patients who are taking beta-blockers. Patients on non-selective beta blockers may be more reactive to allergens given for testing or treatment and may be unresponsive to the usual doses of epinephrine used to treat allergic reactions.
Carcinogenesis, mutagenesis, impairment of fertility:
Long term studies in animals have not been conducted with allergenic extracts to determine their potential carcinogenicity, mutagenicity or impairment of fertility.
Pregnancy: Category C: Animal reproduction studies have not been conducted with Allergenic Extracts. It is not known whether allergenic extracts can cause fetal harm when administered to pregnant women or can affect reproduction capacity. Allergenic extracts should be given to pregnant women only if clearly needed.
Nursing Mothers: It is not known whether this drug appears in human milk. Because many drugs are detected in human milk, caution should be exercised when Allergenic Extracts are administered to a nursing woman. There are no current studies on extract components in human milk, or their effect on the nursing infant.
Pediatric Use: Allergenic extracts have been used in children over two years of age.(5)
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ADVERSE REACTIONS
Adverse systemic reactions usually occur within minutes and consist primarily of allergic symptoms such as: generalized skin erythema, urticaria, pruritus, angioedema, rhinitis, wheezing, laryngeal edema, itching of nose and throat, breathlessness, dyspnea, coughing, hypotension and marked perspiration. Less commonly, nausea, emesis, abdominal cramps, diarrhea and uterine contractions may occur. Severe reactions may cause anaphylaxis or shock and loss of consciousness and rarely death.
The treatment of systemic allergic reactions is dependent upon the system complex. Antihistamines may offer relief of recurrent urticaria, associated skin reactions and gastrointestinal symptoms. Corticosteroids may provide benefit if symptoms are prolonged or recurrent. (See Overdose section)
Local Reactions consisting of erythema, itching, swelling tenderness and sometimes pain may occur at the injection site. These reactions may appear within a few minutes to hours and persist for several days. Local cold applications and oral antihistamines may be effective treatment. For marked and prolonged local reactions the use of antihistamines or anti-inflammatory medications may be dictated. Serious adverse reactions should be reported to Nelco Laboratories immediately and a report can be filed to: MedWatch, The FDA Medical Product Problem Reporting Program, at 5600 Fishers Lane, Rockville, MD 20852-9787, call 1-800-FDA-1088.
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OVERDOSAGE
Overdose can cause both local and systemic reactions. An overdose may be prevented by careful observation and questioning of the patient about the previous injection.
If systemic or anaphylactic reaction, does occur, apply a tourniquet above the site of injection and inject intramuscularly or subcutaneously 0.3 to 0.5ml of 1:1000 Epinephrine Hydrochloride into the opposite arm. The dose may be repeated in 5-10 minutes if necessary. Loosen the tourniquet at least every 10 minutes. The Epinephrine Hydrochloride 1:1000 dose for infants to 2 years is 0.05 to 0.1 ml, for children 2 to 6 years it is 0.15 ml, for children 6-12 years it is 0.2 ml.
Patients unresponsive to Epinephrine may be treated with Theophylline. Studies on asthmatic subjects reveal that plasma concentrations of Theophylline of 5 to 20 µg/ml are associated with therapeutic effects. Toxicity is particularly apparent at concentrations greater than 20 µg/ml. A loading dose of Aminophylline of 5.8 mg/kg intravenously followed by 0.9 mg/kg per hour results in plasma concentrations of approximately 10 µg/ml for patients not previously receiving theophylline. (Mitenko and Ogilive, Nicholoson and Chick,1973)
Other beta-adrenergic drugs such as Isoproterenol, Isoetharine, or Albuterol may be used by inhalation. The usual dose to relieve broncho-constriction in asthma is 0.5 ml of the 0.5% solution for Isoproterenol HCl. The Albuterol inhaler delivers approximately 90 mcg of Albuterol from the mouthpiece. The usual dosage for adults and children would be two inhalations repeated every 4-6 hours. Isoetharine supplied in the Bronkometer unit delivers approximately 340 mcg Isoetharine. The average dose is one to two inhalations. Respiratory obstruction not responding to parenteral or inhaled bronchodilators may require oxygen, intubation and the use of life support systems.
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DOSAGE AND ADMINISTRATION
Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration whenever solution and container permits.
The dosage of allergenic extracts is dependent upon the purpose of the administration. Allergenic extracts can be administered for diagnostic use or for therapeutic use.
When allergenic extracts are administered for diagnostic use, the dosage is dependent upon the method used. Two methods commonly used are scratch testing and intradermal testing. Both types of tests result in a wheal and flare response at the site of the test which usually develops rapidly and may be read in 20-30 minutes.
Diagnostic Use: Scratch Testing Method
Scratch testing is considered a simple and safe method although less sensitive than the intradermal test. Scratch testing can be used to determine the degree of sensitivity to a suspected allergen before using the intradermal test. This combination lessens the severity of response to an allergen which can occur in a very sensitive patient.
The most satisfactory testing site is the patient's back or volar surface of the arms from the axilla to 2.5 or 5cm above the wrist, skipping the anti-cubital space. If using the back as a testing site, the most satisfactory area are from the posterior axillary fold to 2.5 cm from the spinal column, and from the top of the scapula to the lower rib margins.
Allergenic extracts for diagnostic use are to be administered in the following manner: To scratch surface of skin, use a circular scarifier. Do not draw blood. Tests sites should be 4 cm apart to allow for wheal and flare reaction. 1-30 scratch tests may be done at a time. A separate sterile scratch instrument is to be used on each patient to prevent transmission of homologous serum hepatitis or other infectious agents from one patient to another.
The recommended usual dosage for Scratch testing is one drop of allergen applied to each scratch site. Do not let dropper touch skin. Always apply a control scratch with each test set. Sterile Diluent (for a negative control) is used in exactly the same way as an active test extract. Histamine may be used as a positive control. Scratch or prick test sites should be examined at 15 and 30 minutes. To prevent excessive absorption, wipe off antigens producing large reactions as soon as the wheal appears. Record the size of the reaction.
Interpretation of Scratch Test
Skin tests are graded in terms of the wheal and erythema response noted at 10 to 20 minutes. Wheal and erythema size may be recorded by actual measurement as compared with positive and negative controls. A positive reaction consists of an area of erythema surrounding the scarification that is larger than the control site. For uniformity in reporting reactions, the following system is recommended. (6)
REACTION SYMBOL CRITERIA Negative - No wheal. Erythema absent or very slight (not more than 1 mm diameter). One Plus + Wheal absent or very slight erythema present (not more than 3 mm diameter). Two Plus ++ Wheal not more than 3mm or erythema not more than 5mm diameter. Three Plus +++ Wheal between 3mm and 5mm diameter, with erythema. Possible pseudopodia and itching. Four Plus ++++ A larger reaction with itching and pain. Diagnostic Use: Intradermal Skin Testing Method
Do not perform intradermal test with allergens which have evoked a 2+ or greater response to a Scratch test. Clean test area with alcohol, place sites 5 cm apart using separate sterile tuberculin syringe and a 25 gauge needle for each allergen. Insert needle tip, bevel up, into intracutaneous space. Avoid injecting into blood vessel, pull back gently on syringe plunger, if blood enters syringe change position of needle. The recommended dosage and range for intradermal testing is 0.05 ml of not more than 100 pnu/ml or 1:1000 w/v (only if puncture test is negative) of allergenic extract. Inject slowly until a small bleb is raised. It is important to make each bleb the same size.
Interpretation of Intradermal Test:
The patient's reaction is graded on the basis of size of wheal and flare as compared to control. Use 0.05 ml sterile diluent as a negative control to give accurate interpretation. The tests may be accurately interpreted only when the saline control site has shown a negative response. Observe patient for at least 30 minutes. Tests can be read in 15-20 minutes. Edema, erythema and presence of pseudopods, pain and itching may be observed in 4 plus reactions. For uniformity in reporting reactions the following system is recommended. (6)
REACTION SYMBOL CRITERIA Negative - No increase in size of bleb since injection. No erythema. One Plus + An increase in size of bleb to a wheal not more than 5mm diameter, with associated erythema. Two Plus ++ Wheal between 5mm and 8mm diameter with erythema. Three Plus +++ Wheal between 8mm and 12mm diameter with erythema and possible pseudopodia and itching or pain. Four Plus ++++ Any larger reaction with itch and pain, and possible diffuse blush of the skin surrounding the reaction area. Therapeutic Use: Recommended dosage & range
Check the listed ingredients to verify that it matches the prescription ordered. When using a prescription set, verify the patient's name and the ingredients listed with the prescription order. Assess the patient's physical and emotional status prior to giving as injection. Do not give injections to patients who are in acute distress. Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit.
Dosage of allergenic extracts is a highly individualized matter and varies according to the degree of sensitivity of the patient, his clinical response and tolerance to the extract administered during the early phases of an injection regimen. The dosage must be reduced when transferring a patient from non-standardized or modified extract to standardized extract. Any evidence of a local or generalized reaction requires a reduction in dosage during the initial stages of immunotherapy as well as during maintenance therapy. After therapeutic injections patients should be observed for at least 20 minutes for reaction symptoms.
The following schedule may act as a guide. This schedule has not been proven to be safe or effective. Sensitive patients may begin with smaller doses of weaker solutions and the dosage increments can be less.
STRENGTH DOSE VOLUME Vial #1 1 0.05 1:100,000 w/v 2 0.10 10 pnu/ml 3 0.15 1 AU/ml 4 0.20 1 BAU/ml 5 0.30 6 0.40 7 0.50 Vial #2 8 0.05 1:10,000 w/v 9 0.10 100 pnu/ml 10 0.15 10 AU/ml 11 0.20 10 BAU/ml 12 0.30 13 0.40 14 0.50 Vial #3 15 0.05 1:1,000 w/v 16 0.10 1,000 pnu/ml 17 0.15 100 AU/ml 18 0.20 100 BAU/ml 19 0.30 20 0.40 21 0.50 Vial #4 22 0.05 1:100 w/v 23 0.07 10,000 pnu/ml 24 0.10 1,000 AU/ml 25 0.15 1,000 BAU/ml 26 0.20 27 0.25 Maintenance Refill 28 0.25 1:100 w/v 29 0.25 10,000 pnu/ml 30 0.25 1,000 AU/ml 31 0.25 1,000 BAU/ml 32 0.25 subsequent doses 33 0.25 All dilutions may be made using sterile buffered diluent. The calculation may be based on the following ratio:
Volume desired x Concentration desired = Volume needed x Concentration available.
Example 1: If a 1:10 w/v extract is available and it is desired to use a 1:1,000 w/v extract substitute as follows:
Using a sterile technique, remove 0.10 ml of extract from the 1:10 vial and place it into a vial containing 9.90 ml of sterile diluent. The resulting ratio will be a 10 ml vial of 1:1,000 w/v.
Example 2: If a 10,000 pnu/ml extract is available and it is desired to use a 100 pnu/ml extract substitute as follows:
Using a sterile technique, remove 0.10 ml of extract from the 10,000 pnu/ml vial and place it into a vial containing 9.90 ml of sterile diluent. The resulting concentration will be a 10 ml vial of 100 pnu/ml.
Example 3: If a 10,000 AU/ml or BAU/ml extract is available and it is desired to use a 100 AU/ml or BAU/ml extract substitute as follows: Vd x Cd = Vn x Ca
Using a sterile technique, remove 0.10 ml of extract from the 10,000 AU/ml or BAU/ml vial and place it into a vial containing 9.90 ml of sterile diluent. The resulting concentration will be 10ml vial of 100 AU/ml or BAU/ml.
Intervals between doses: The optimal interval between doses of allergenic extract has not been definitely established. The amount of allergenic extract is increased at each injection by not more than 50%-100% of the previous amount and the next increment is governed by the response to the last injection. There are three generally accepted methods of pollen hyposensitizing therapy.
Treatment starts each year 6 to 8 weeks before onset of seasonal symptoms. Maximal dose reached just before symptoms are expected. Injections discontinued during and following season until next year.
Patient is first treated during season with symptoms. Low initial doses are employed to prevent worsening of condition. This is followed by an intensive schedule of therapy (i.e. injections given 2 to 3 times per week). Fewer Allergists are resorting to this Co-seasonal therapy because of the availability of more effective, symptomatic medications that allow the patient to go through a season relatively symptom free.
Initially this is the same as pre seasonal. The allergen is administered twice weekly or weekly for about 20 injections to achieve the maximum tolerated dose. Then, maintenance therapy may be administered once a week or less frequently.
Duration of Treatment: The usual duration of treatment has not been established. A period of two or three years of injection therapy constitutes an average minimum course of treatment.
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HOW SUPPLIED
Allergenic extracts are supplied with units listed as: Weight/volume (W/V), Protein Nitrogen Units (PNU/ml), Allergy Units (AU/ml) or Bioequivalent Allergy Units (BAU/ml).
Diagnostic Scratch: 5 ml dropper application vials
Diagnostic Intradermal: 5 ml or 10 ml vials.
Therapeutic Allergens: 5 ml, 10 ml, 50 ml multiple dose vials.
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STORAGE
The expiration date of allergen extracts is listed on the container label. Store extracts upon arrival at 2° to 8°C and keep them in this range during office use.
WARRANTY:We warrant that this product was prepared and tested according to the standards of the FDA and is true to label. Because of biological differences in individuals and because allergenic extracts are manufactured to be potent and because we have no control over the conditions of use, we cannot and do not warrant either a good effect or against an ill effect following use.
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REFERENCES
1 Jacobs, Robert L., Geoffrey W.Rake,Jr., et.al. Potentiated Anaphylaxis in Patients with Drug-induced Beta-adrenergic Blockade. J.Allergy & Clin. Immunol., 68(2): 125-127. August 1981.
2 Ishizaka,K.: Cellular Events in the IgE Antibody Response. Adv. in Immuno. 23:50-75, 1976.
3. Lockey, R.F., Bukantz, S.C., Allergen Immunotherapy. New York,NY: Marcel Dekker Inc., 1991.
4. Reid,M.J., Lockey,R.F., Turkeltaub,P.C., Platts-Mills,T.A.E., Survey of fatalities from skin testing and immunotherapy 1985-1989. Journal of Allergy Clin. Immunol. 92 (1): 6-15, July 1993.
5. Murray, A.B., Ferguson, A., Morrison, B., The frequency and severity of cat allergy vs dog allergy in atopic children. J. Allergy Clin. Immunolo: 72, 145-9, 1983.
6. Lockey, R.F., Bukantz, S.C., Allergen Immunotherapy. New York,NY: Marcel Dekker Inc., 1991.
- CONTAINER LABELING
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INGREDIENTS AND APPEARANCE
CARPÂ
carp injection, solutionProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1197 Route of Administration INTRADERMAL, SUBCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength COMMON CARP (UNII: ZB2SV6JJY5) (COMMON CARP - UNII:ZB2SV6JJY5) COMMON CARP 0.1 g  in 1 mL Inactive Ingredients Ingredient Name Strength SODIUM CHLORIDE (UNII: 451W47IQ8X)  SODIUM BICARBONATE (UNII: 8MDF5V39QO)  PHENOL (UNII: 339NCG44TV)  WATER (UNII: 059QF0KO0R)  GLYCERIN (UNII: PDC6A3C0OX)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:36987-1197-1 5 mL in 1 VIAL, MULTI-DOSE 2 NDC:36987-1197-2 10 mL in 1 VIAL, MULTI-DOSE 3 NDC:36987-1197-3 30 mL in 1 VIAL, MULTI-DOSE 4 NDC:36987-1197-4 50 mL in 1 VIAL, MULTI-DOSE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA102192 08/29/1972 CLAMÂ
clam injection, solutionProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1201 Route of Administration INTRADERMAL, SUBCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CLAM (UNII: 226LY0AFR9) (CLAM - UNII:226LY0AFR9) CLAM 0.1 g  in 1 mL Inactive Ingredients Ingredient Name Strength SODIUM CHLORIDE (UNII: 451W47IQ8X)  SODIUM BICARBONATE (UNII: 8MDF5V39QO)  PHENOL (UNII: 339NCG44TV)  WATER (UNII: 059QF0KO0R)  GLYCERIN (UNII: PDC6A3C0OX)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:36987-1201-1 5 mL in 1 VIAL, MULTI-DOSE 2 NDC:36987-1201-2 10 mL in 1 VIAL, MULTI-DOSE 3 NDC:36987-1201-3 30 mL in 1 VIAL, MULTI-DOSE 4 NDC:36987-1201-4 50 mL in 1 VIAL, MULTI-DOSE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA102192 08/29/1972 CODFISHÂ
codfish injection, solutionProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1205 Route of Administration INTRADERMAL, SUBCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CODFISH (UNII: 8D6Q5LNG3D) (CODFISH - UNII:8D6Q5LNG3D) CODFISH 0.1 g  in 1 mL Inactive Ingredients Ingredient Name Strength SODIUM CHLORIDE (UNII: 451W47IQ8X)  SODIUM BICARBONATE (UNII: 8MDF5V39QO)  PHENOL (UNII: 339NCG44TV)  WATER (UNII: 059QF0KO0R)  GLYCERIN (UNII: PDC6A3C0OX)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:36987-1205-1 5 mL in 1 VIAL, MULTI-DOSE 2 NDC:36987-1205-2 10 mL in 1 VIAL, MULTI-DOSE 3 NDC:36987-1205-3 30 mL in 1 VIAL, MULTI-DOSE 4 NDC:36987-1205-4 50 mL in 1 VIAL, MULTI-DOSE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA102192 08/29/1972 CRABÂ
crab injection, solutionProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1209 Route of Administration INTRADERMAL, SUBCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CRAB (UNII: S1VF61QLO9) (CRAB - UNII:S1VF61QLO9) CRAB 0.1 g  in 1 mL Inactive Ingredients Ingredient Name Strength SODIUM CHLORIDE (UNII: 451W47IQ8X)  SODIUM BICARBONATE (UNII: 8MDF5V39QO)  PHENOL (UNII: 339NCG44TV)  WATER (UNII: 059QF0KO0R)  GLYCERIN (UNII: PDC6A3C0OX)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:36987-1209-1 5 mL in 1 VIAL, MULTI-DOSE 2 NDC:36987-1209-2 10 mL in 1 VIAL, MULTI-DOSE 3 NDC:36987-1209-3 30 mL in 1 VIAL, MULTI-DOSE 4 NDC:36987-1209-4 50 mL in 1 VIAL, MULTI-DOSE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA102192 08/29/1972 FLOUNDERÂ
flounder injection, solutionProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1213 Route of Administration INTRADERMAL, SUBCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength FLOUNDER (UNII: T197LO581X) (FLOUNDER - UNII:T197LO581X) FLOUNDER 0.1 g  in 1 mL Inactive Ingredients Ingredient Name Strength SODIUM CHLORIDE (UNII: 451W47IQ8X)  SODIUM BICARBONATE (UNII: 8MDF5V39QO)  PHENOL (UNII: 339NCG44TV)  WATER (UNII: 059QF0KO0R)  GLYCERIN (UNII: PDC6A3C0OX)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:36987-1213-1 5 mL in 1 VIAL, MULTI-DOSE 2 NDC:36987-1213-2 10 mL in 1 VIAL, MULTI-DOSE 3 NDC:36987-1213-3 30 mL in 1 VIAL, MULTI-DOSE 4 NDC:36987-1213-4 50 mL in 1 VIAL, MULTI-DOSE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA102192 08/29/1972 HADDOCKÂ
haddock injection, solutionProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1217 Route of Administration INTRADERMAL, SUBCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HADDOCK (UNII: 0WLY635722) (HADDOCK - UNII:0WLY635722) HADDOCK 0.1 g  in 1 mL Inactive Ingredients Ingredient Name Strength SODIUM CHLORIDE (UNII: 451W47IQ8X)  SODIUM BICARBONATE (UNII: 8MDF5V39QO)  PHENOL (UNII: 339NCG44TV)  WATER (UNII: 059QF0KO0R)  GLYCERIN (UNII: PDC6A3C0OX)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:36987-1217-1 5 mL in 1 VIAL, MULTI-DOSE 2 NDC:36987-1217-2 10 mL in 1 VIAL, MULTI-DOSE 3 NDC:36987-1217-3 30 mL in 1 VIAL, MULTI-DOSE 4 NDC:36987-1217-4 50 mL in 1 VIAL, MULTI-DOSE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA102192 08/29/1972 HALIBUTÂ
halibut injection, solutionProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1221 Route of Administration INTRADERMAL, SUBCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PACIFIC HALIBUT (UNII: BKZ683617P) (PACIFIC HALIBUT - UNII:BKZ683617P) PACIFIC HALIBUT 0.1 g  in 1 mL Inactive Ingredients Ingredient Name Strength SODIUM CHLORIDE (UNII: 451W47IQ8X)  SODIUM BICARBONATE (UNII: 8MDF5V39QO)  PHENOL (UNII: 339NCG44TV)  WATER (UNII: 059QF0KO0R)  GLYCERIN (UNII: PDC6A3C0OX)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:36987-1221-1 5 mL in 1 VIAL, MULTI-DOSE 2 NDC:36987-1221-2 10 mL in 1 VIAL, MULTI-DOSE 3 NDC:36987-1221-3 30 mL in 1 VIAL, MULTI-DOSE 4 NDC:36987-1221-4 50 mL in 1 VIAL, MULTI-DOSE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA102192 08/29/1972 HERRINGÂ
herring injection, solutionProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1225 Route of Administration INTRADERMAL, SUBCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HERRING (UNII: 34EX28T4C1) (HERRING - UNII:34EX28T4C1) HERRING 0.1 g  in 1 mL Inactive Ingredients Ingredient Name Strength SODIUM CHLORIDE (UNII: 451W47IQ8X)  SODIUM BICARBONATE (UNII: 8MDF5V39QO)  PHENOL (UNII: 339NCG44TV)  WATER (UNII: 059QF0KO0R)  GLYCERIN (UNII: PDC6A3C0OX)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:36987-1225-1 5 mL in 1 VIAL, MULTI-DOSE 2 NDC:36987-1225-2 10 mL in 1 VIAL, MULTI-DOSE 3 NDC:36987-1225-3 30 mL in 1 VIAL, MULTI-DOSE 4 NDC:36987-1225-4 50 mL in 1 VIAL, MULTI-DOSE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA102192 08/29/1972 LOBSTERÂ
lobster injection, solutionProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1229 Route of Administration INTRADERMAL, SUBCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LOBSTER (UNII: ZQ6LG2C39M) (LOBSTER - UNII:ZQ6LG2C39M) LOBSTER 0.1 g  in 1 mL Inactive Ingredients Ingredient Name Strength SODIUM CHLORIDE (UNII: 451W47IQ8X)  SODIUM BICARBONATE (UNII: 8MDF5V39QO)  PHENOL (UNII: 339NCG44TV)  WATER (UNII: 059QF0KO0R)  GLYCERIN (UNII: PDC6A3C0OX)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:36987-1229-1 5 mL in 1 VIAL, MULTI-DOSE 2 NDC:36987-1229-2 10 mL in 1 VIAL, MULTI-DOSE 3 NDC:36987-1229-3 30 mL in 1 VIAL, MULTI-DOSE 4 NDC:36987-1229-4 50 mL in 1 VIAL, MULTI-DOSE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA102192 08/29/1972 MACKERELÂ
mackerel injection, solutionProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1233 Route of Administration INTRADERMAL, SUBCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MACKEREL (UNII: CYO6K3VM7F) (MACKEREL - UNII:CYO6K3VM7F) MACKEREL 0.1 g  in 1 mL Inactive Ingredients Ingredient Name Strength SODIUM CHLORIDE (UNII: 451W47IQ8X)  SODIUM BICARBONATE (UNII: 8MDF5V39QO)  PHENOL (UNII: 339NCG44TV)  WATER (UNII: 059QF0KO0R)  GLYCERIN (UNII: PDC6A3C0OX)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:36987-1233-1 5 mL in 1 VIAL, MULTI-DOSE 2 NDC:36987-1233-2 10 mL in 1 VIAL, MULTI-DOSE 3 NDC:36987-1233-3 30 mL in 1 VIAL, MULTI-DOSE 4 NDC:36987-1233-4 50 mL in 1 VIAL, MULTI-DOSE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA102192 08/29/1972 OYSTERÂ
oyster injection, solutionProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1237 Route of Administration INTRADERMAL, SUBCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OYSTER (UNII: S614XWR17V) (OYSTER - UNII:S614XWR17V) OYSTER 0.1 g  in 1 mL Inactive Ingredients Ingredient Name Strength SODIUM CHLORIDE (UNII: 451W47IQ8X)  SODIUM BICARBONATE (UNII: 8MDF5V39QO)  PHENOL (UNII: 339NCG44TV)  WATER (UNII: 059QF0KO0R)  GLYCERIN (UNII: PDC6A3C0OX)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:36987-1237-1 5 mL in 1 VIAL, MULTI-DOSE 2 NDC:36987-1237-2 10 mL in 1 VIAL, MULTI-DOSE 3 NDC:36987-1237-3 30 mL in 1 VIAL, MULTI-DOSE 4 NDC:36987-1237-4 50 mL in 1 VIAL, MULTI-DOSE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA102192 08/29/1972 RED SNAPPERÂ
red snapper injection, solutionProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1245 Route of Administration INTRADERMAL, SUBCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength RED SNAPPER (UNII: WF621S7K14) (RED SNAPPER - UNII:WF621S7K14) RED SNAPPER 0.1 g  in 1 mL Inactive Ingredients Ingredient Name Strength SODIUM CHLORIDE (UNII: 451W47IQ8X)  SODIUM BICARBONATE (UNII: 8MDF5V39QO)  PHENOL (UNII: 339NCG44TV)  WATER (UNII: 059QF0KO0R)  GLYCERIN (UNII: PDC6A3C0OX)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:36987-1245-1 5 mL in 1 VIAL, MULTI-DOSE 2 NDC:36987-1245-2 10 mL in 1 VIAL, MULTI-DOSE 3 NDC:36987-1245-3 30 mL in 1 VIAL, MULTI-DOSE 4 NDC:36987-1245-4 50 mL in 1 VIAL, MULTI-DOSE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA102192 08/29/1972 SALMONÂ
salmon injection, solutionProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1249 Route of Administration INTRADERMAL, SUBCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ATLANTIC SALMON (UNII: 7062I37LB3) (ATLANTIC SALMON - UNII:7062I37LB3) ATLANTIC SALMON 0.1 g  in 1 mL Inactive Ingredients Ingredient Name Strength SODIUM CHLORIDE (UNII: 451W47IQ8X)  SODIUM BICARBONATE (UNII: 8MDF5V39QO)  PHENOL (UNII: 339NCG44TV)  WATER (UNII: 059QF0KO0R)  GLYCERIN (UNII: PDC6A3C0OX)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:36987-1249-1 5 mL in 1 VIAL, MULTI-DOSE 2 NDC:36987-1249-2 10 mL in 1 VIAL, MULTI-DOSE 3 NDC:36987-1249-3 30 mL in 1 VIAL, MULTI-DOSE 4 NDC:36987-1249-4 50 mL in 1 VIAL, MULTI-DOSE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA102192 08/29/1972 SARDINEÂ
sardine injection, solutionProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1253 Route of Administration INTRADERMAL, SUBCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength EUROPEAN PILCHARD (UNII: 76780GX08D) (EUROPEAN PILCHARD - UNII:76780GX08D) EUROPEAN PILCHARD 0.1 g  in 1 mL Inactive Ingredients Ingredient Name Strength SODIUM CHLORIDE (UNII: 451W47IQ8X)  SODIUM BICARBONATE (UNII: 8MDF5V39QO)  PHENOL (UNII: 339NCG44TV)  WATER (UNII: 059QF0KO0R)  GLYCERIN (UNII: PDC6A3C0OX)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:36987-1253-1 5 mL in 1 VIAL, MULTI-DOSE 2 NDC:36987-1253-2 10 mL in 1 VIAL, MULTI-DOSE 3 NDC:36987-1253-3 30 mL in 1 VIAL, MULTI-DOSE 4 NDC:36987-1253-4 50 mL in 1 VIAL, MULTI-DOSE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA102192 08/29/1972 SCALLOPÂ
scallop injection, solutionProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1257 Route of Administration INTRADERMAL, SUBCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SCALLOP (UNII: D380C73WOU) (SCALLOP - UNII:D380C73WOU) SCALLOP 0.1 g  in 1 mL Inactive Ingredients Ingredient Name Strength SODIUM CHLORIDE (UNII: 451W47IQ8X)  SODIUM BICARBONATE (UNII: 8MDF5V39QO)  PHENOL (UNII: 339NCG44TV)  WATER (UNII: 059QF0KO0R)  GLYCERIN (UNII: PDC6A3C0OX)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:36987-1257-1 5 mL in 1 VIAL, MULTI-DOSE 2 NDC:36987-1257-2 10 mL in 1 VIAL, MULTI-DOSE 3 NDC:36987-1257-3 30 mL in 1 VIAL, MULTI-DOSE 4 NDC:36987-1257-4 50 mL in 1 VIAL, MULTI-DOSE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA102192 08/29/1972 SHRIMPÂ
shrimp injection, solutionProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1261 Route of Administration INTRADERMAL, SUBCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SHRIMP (UNII: 1891LE191T) (SHRIMP - UNII:1891LE191T) SHRIMP 0.1 g  in 1 mL Inactive Ingredients Ingredient Name Strength SODIUM CHLORIDE (UNII: 451W47IQ8X)  SODIUM BICARBONATE (UNII: 8MDF5V39QO)  PHENOL (UNII: 339NCG44TV)  WATER (UNII: 059QF0KO0R)  GLYCERIN (UNII: PDC6A3C0OX)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:36987-1261-1 5 mL in 1 VIAL, MULTI-DOSE 2 NDC:36987-1261-2 10 mL in 1 VIAL, MULTI-DOSE 3 NDC:36987-1261-3 30 mL in 1 VIAL, MULTI-DOSE 4 NDC:36987-1261-4 50 mL in 1 VIAL, MULTI-DOSE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA102192 08/29/1972 SWORD FISHÂ
sword fish injection, solutionProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1269 Route of Administration INTRADERMAL, SUBCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SWORDFISH (UNII: 01695YPV36) (SWORDFISH - UNII:01695YPV36) SWORDFISH 0.1 g  in 1 mL Inactive Ingredients Ingredient Name Strength SODIUM CHLORIDE (UNII: 451W47IQ8X)  SODIUM BICARBONATE (UNII: 8MDF5V39QO)  PHENOL (UNII: 339NCG44TV)  WATER (UNII: 059QF0KO0R)  GLYCERIN (UNII: PDC6A3C0OX)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:36987-1269-1 5 mL in 1 VIAL, MULTI-DOSE 2 NDC:36987-1269-2 10 mL in 1 VIAL, MULTI-DOSE 3 NDC:36987-1269-3 30 mL in 1 VIAL, MULTI-DOSE 4 NDC:36987-1269-4 50 mL in 1 VIAL, MULTI-DOSE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA102192 08/29/1972 TROUTÂ
trout injection, solutionProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1273 Route of Administration INTRADERMAL, SUBCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TROUT (UNII: 7TI7U5PF2U) (TROUT - UNII:7TI7U5PF2U) TROUT 0.1 g  in 1 mL Inactive Ingredients Ingredient Name Strength SODIUM CHLORIDE (UNII: 451W47IQ8X)  SODIUM BICARBONATE (UNII: 8MDF5V39QO)  PHENOL (UNII: 339NCG44TV)  WATER (UNII: 059QF0KO0R)  GLYCERIN (UNII: PDC6A3C0OX)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:36987-1273-1 5 mL in 1 VIAL, MULTI-DOSE 2 NDC:36987-1273-2 10 mL in 1 VIAL, MULTI-DOSE 3 NDC:36987-1273-3 30 mL in 1 VIAL, MULTI-DOSE 4 NDC:36987-1273-4 50 mL in 1 VIAL, MULTI-DOSE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA102192 08/29/1972 TUNA FISHÂ
tuna fish injection, solutionProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1277 Route of Administration INTRADERMAL, SUBCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TUNA (UNII: V2T3IHT3E2) (TUNA - UNII:V2T3IHT3E2) TUNA 0.1 g  in 1 mL Inactive Ingredients Ingredient Name Strength SODIUM CHLORIDE (UNII: 451W47IQ8X)  SODIUM BICARBONATE (UNII: 8MDF5V39QO)  PHENOL (UNII: 339NCG44TV)  WATER (UNII: 059QF0KO0R)  GLYCERIN (UNII: PDC6A3C0OX)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:36987-1277-1 5 mL in 1 VIAL, MULTI-DOSE 2 NDC:36987-1277-2 10 mL in 1 VIAL, MULTI-DOSE 3 NDC:36987-1277-3 30 mL in 1 VIAL, MULTI-DOSE 4 NDC:36987-1277-4 50 mL in 1 VIAL, MULTI-DOSE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA102192 08/29/1972 WHITE FISHÂ
white fish injection, solutionProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1281 Route of Administration INTRADERMAL, SUBCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength WHITE FISH (UNII: IA4C8ND0DT) (WHITE FISH - UNII:IA4C8ND0DT) WHITE FISH 0.1 g  in 1 mL Inactive Ingredients Ingredient Name Strength SODIUM CHLORIDE (UNII: 451W47IQ8X)  SODIUM BICARBONATE (UNII: 8MDF5V39QO)  PHENOL (UNII: 339NCG44TV)  WATER (UNII: 059QF0KO0R)  GLYCERIN (UNII: PDC6A3C0OX)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:36987-1281-1 5 mL in 1 VIAL, MULTI-DOSE 2 NDC:36987-1281-2 10 mL in 1 VIAL, MULTI-DOSE 3 NDC:36987-1281-3 30 mL in 1 VIAL, MULTI-DOSE 4 NDC:36987-1281-4 50 mL in 1 VIAL, MULTI-DOSE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA102192 08/29/1972 PIKEÂ
pike injection, solutionProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1241 Route of Administration INTRADERMAL, SUBCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NORTHERN PIKE (UNII: 5JKY494U4L) (NORTHERN PIKE - UNII:5JKY494U4L) NORTHERN PIKE 0.1 g  in 1 mL Inactive Ingredients Ingredient Name Strength SODIUM CHLORIDE (UNII: 451W47IQ8X)  SODIUM BICARBONATE (UNII: 8MDF5V39QO)  WATER (UNII: 059QF0KO0R)  PHENOL (UNII: 339NCG44TV)  GLYCERIN (UNII: PDC6A3C0OX)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:36987-1241-1 5 mL in 1 VIAL, MULTI-DOSE 2 NDC:36987-1241-2 10 mL in 1 VIAL, MULTI-DOSE 3 NDC:36987-1241-3 30 mL in 1 VIAL, MULTI-DOSE 4 NDC:36987-1241-4 50 mL in 1 VIAL, MULTI-DOSE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA102192 08/29/1972 SMELTÂ
smelt injection, solutionProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1265 Route of Administration INTRADERMAL, SUBCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SMELT (UNII: 9VVF5SCM9I) (SMELT - UNII:9VVF5SCM9I) SMELT 0.1 g  in 1 mL Inactive Ingredients Ingredient Name Strength SODIUM CHLORIDE (UNII: 451W47IQ8X)  SODIUM BICARBONATE (UNII: 8MDF5V39QO)  WATER (UNII: 059QF0KO0R)  PHENOL (UNII: 339NCG44TV)  GLYCERIN (UNII: PDC6A3C0OX)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:36987-1265-1 5 mL in 1 VIAL, MULTI-DOSE 2 NDC:36987-1265-2 10 mL in 1 VIAL, MULTI-DOSE 3 NDC:36987-1265-3 30 mL in 1 VIAL, MULTI-DOSE 4 NDC:36987-1265-4 50 mL in 1 VIAL, MULTI-DOSE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date BLA BLA102192 08/29/1972 Labeler - Nelco Laboratories, Inc. (054980867) Registrant - Nelco Laboratories, Inc. (054980867) Establishment Name Address ID/FEI Business Operations Nelco Laboratories, Inc. 054980867 manufacture