Dexamethasone Sodium Phosphate 4 mg/mL Injection, USP 30 mL Multi Dose Vial

DEXAMETHASONE SODIUM PHOSPHATE  - dexamethasone sodium phosphate injection, suspension 
General Injectables & Vaccines

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Dexamethasone Sodium Phosphate 4 mg/mL Injection, USP 30 mL Multi Dose Vial

Description

Dexamethasone Sodium Phosphate Injection, USP is a water-soluble inorganic ester of dexamethasone.
It occurs as a yellow crystalline powder, is odorless or has a slight odor of alcohol, is exceedingly hygroscopic, and is freely soluble in water.
Dexamethasone Sodium Phosphate Injection, USP is a synthetic adrenocortical steroid anti-inflammatory drug.
It has the following structural formula:


Formula

Dexamethasone Sodium Phosphate Injection, USP C22H28FNa2O8P, has a molecular weight of 516.41 and the chemical name 9- fluoro-11b,17,21-trihydroxy-16a-methylpregna-1,4-diene-3,20-dione 21-(dihydrogen phosphate) disodium salt. Dexamethasone Sodium Phosphate Injection, USP 4 mg/mL is a sterile solution for intravenous, intramuscular, intra-articular, intralesional and soft tissue administration.
Each mL of the injection contains the following components:
  

    Dexamethasone Sodium Phosphate

    (equivalent to 4 mg of Dexamethasone Phosphate)...4.37 mg

    Sodium Sulfite.............................................................1 mg

    Benzyl Alcohol.............................................................10 mg

    Sodium Citrate.............................................................for isotonicity

    Water for Injection........................................................q.s.

    pH adjusted between 7.5 and 10.5 with Citric Acid and/or Sodium Hydroxide.

Clinical Pharmacology

Dexamethasone Sodium Phosphate Injection, USP has a rapid onset but short duration of action when compared with less soluble preparations. Because of this, it is suitable for the treatment of acute disorders responsive to adrenocortical steroid therapy. Naturally occurring glucocorticoids (hydrocortisone and cortisone), which also have salt-retaining properties, are used as replacement therapy in adrenocortical deficiency states. Their synthetic analogs, including dexamethasone, are primarily used for their potent antiinflammatory effects in disorders of many organ systems. Glucocorticoids cause profound and varied metabolic effects. In addition, they modify the body's immune responses to diverse stimuli. At equipotent anti-inflammatory doses, dexamethasone almost completely lacks the sodium-retaining property of hydrocortisone and closely related derivatives of hydrocortisone.

Indications and Usage

1. By intravenous or intramuscular injection when oral therapy is not feasible:
1. Endocrine disorders
    Primary or secondary adrenocortical insufficiency (hydrocortisone or cortisone is the drug of choice; synthetic analogs may be     used in conjunction with mineralocorticoids where             applicable; in infancy, mineralocorticoid supplementation is of particular importance)
    Acute adrenocortical insufficiency (hydrocortisone or cortisone is the drug of choice; mineralocorticoid supplementation may be necessary, particularly when synthetic analogs are used)
    Preoperatively, and in the event of serious trauma or illness, in patients with known adrenal insufficiency or when adrenocortical reserve is doubtful
    Shock unresponsive to conventional therapy if adrenocortical insufficiency exists or is suspected
    Congenital adrenal hyperplasia
    Nonsuppurative thyroiditis
    Hypercalcemia associated with cancer
2. Rheumatic disorders
    As adjunctive therapy for short-term administration (to tide the patient over an acute episode or exacerbation) in:
    Post-traumatic osteoarthritis
    Synovitis of osteoarthritis
    Rheumatoid arthritis, including juvenile rheumatoid arthritis (selected cases may require low-dose maintenance therapy)
    Acute and subacute bursitis
    Epicondylitis
    Acute nonspecific tenosynovitis
    Acute gouty arthritis
    Psoriatic arthritis
    Ankylosing spondylitis
3. Collagen diseases
    During an exacerbation or as maintenance therapy in selected cases of:
    Systemic lupus erythematosus
    Acute rheumatic carditis
4. Dermatologic diseases
    Pemphigus
    Severe erythema multiforme (Stevens-Johnson syndrome)
    Exfoliative dermatitis
    Bullous dermatitis herpetiformis
    Severe seborrheic dermatitis
    Severe psoriasis
    Mycosis fungoides
5. Allergic states
    Control of severe or incapacitating allergic conditions intractable to adequate trials of conventional treatment in:
    Bronchial asthma
    Contact dermatitis
    Atopic dermatitis
    Serum sickness
    Seasonal or perennial allergic rhinitis
    Drug hypersensitivity reactions
    Urticarial transfusion reactions
    Acute noninfectious laryngeal edema (epinephrine is the drug of first choice)
6. Ophthalmic diseases
    Severe acute and chronic allergic and inflammatory processes involving the eye, such as:
    Herpes zoster ophthalmicus
    Iritis, iridocyclitis
    Chorioretinitis
    Diffuse posterior uveitis and choroiditis
    Optic neuritis
    Sympathetic ophthalmia
    Anterior segment inflammation
    Allergic conjunctivitis
    Keratitis
    Allergic corneal marginal ulcers
7. Gastrointestinal diseases
    To tide the patient over a critical period of the disease in:
    Ulcerative colitis (Systemic therapy)
    Regional enteritis (Systemic therapy)
8. Respiratory diseases
    Symptomatic sarcoidosis
    Berylliosis
    Fulminating or disseminated pulmonary tuberculosis when used concurrently with appropriate antituberculous chemotherapy
    Loeffler's syndrome not manageable by other means
    Aspiration pneumonitis
9. Hematologic disorders
    Acquired (autoimmune) hemolytic anemia
    Idiopathic thrombocytopenic purpura in adults (I.V. only: I.M administration is contraindicated)
    Secondary thrombocytopenia in adults
    Erythroblastopenia (RBC anemia)
    Congenital (erythroid) hypoplasticanemia
10. Neoplastic diseases
    For palliative management of:
    Leukemias and lymphomas in adults
    Acute leukemia of childhood
11. Edematous states
    To induce diuresis or remission of proteinuria in the nephrotic syndrome, without uremia, of the idiopathic type, or that due to lupus erythematosus
12. Miscellaneous
    Tuberculous meningitis with subarachnoid block or impending block when used concurrently with appropriate antituberculous chemotherapy
    Trichinosis with neurologic or myocardial involvement
13. Diagnostic testing of adrenocortical hyperfunction
14. Cerebral Edema associated with primary or metastatic brain tumor, craniotomy, or head injury. Use in cerebral edema is not a substitute for careful neurosurgical evaluation and                 definitive management such as neurosurgery or other specific therapy.

2. By intra-articular or soft tissue injection:
    As adjunctive therapy for short-term administration (to tide the patient over an acute episode or exacerbation) in:
    Synovitis of osteoarthritis
    Rheumatoid arthritis
    Acute and subacute bursitis
    Acute gouty arthritis
    Epicondylitis
    Acute nonspecific tenosynovitis
    Post-traumatic osteoarthritis.

3. By intralesional injection:
    Keloids
    Localized hypertrophic, infiltrated, inflammatory lesions of: lichen planus, psoriatic plaques, granuloma annulare and lichen simplex chronicus (neurodermatitis)
    Discoid lupus erythematosus
    Necrobiosis lipoidica diabeticorum
    Alopecia areata
    May also be useful in cystic tumors of an aponeurosis or tendon (ganglia).

Contraindications

Systemic fungal infections. (See WARNINGS regarding amphotericin B)
Hypersensitivity to any component of this product, including sulfites (see WARNINGS).

Warnings

Because rare instances of anaphylactoid reactions have occurred in patients receiving parenteral corticosteroid therapy, appropriate precautionary measures should be taken prior to administration, especially when the patient has a history of allergy to any drug. Anaphylactoid and hypersensitivity reactions have been reported for Dexamethasone Sodium Phosphate Injection, USP (see ADVERSE REACTIONS). Dexamethasone Sodium Phosphate Injection, USP contains sodium bisulfite, a sulfite that may cause allergic-type reactions including
anaphylactic symptoms and life-threatening or less severe asthmatic episodes in certain susceptible people. The overall prevalence of sulfite sensitivity in the general population is unknown and probably low. Sulfite sensitivity is seen more frequently in asthmatic than in nonasthmatic people. Corticosteroids may exacerbate systemic fungal infections and therefore should not be used in the presence of such infections unless they are needed to control drug reactions due to amphotericin B. Moreover, there have been cases reported in which concomitant use of amphotericin B and hydrocortisone was followed by cardiac enlargement and congestive failure. In patients on corticosteroid therapy subjected to any unusual stress, increased dosage of rapidly acting corticosteroids before, during, and after the stressful situation is indicated. Drug-induced secondary adrenocortical insufficiency may result from too rapid withdrawal of corticosteroids and may be minimized by gradual reduction of dosage. This type of relative insufficiency may persist for months after discontinuation of therapy; therefore, in any situation of stress occurring during that period, hormone therapy should be reinstituted. If the patient is receiving steroids already, dosage may have to be increased. Since mineralocorticoid secretion may be impaired, salt and/or a mineralocorticoid should be administered concurrently. Corticosteroids may mask some signs of infection, and new infections may appear during their use. There may be decreased resistance and inability to localize infection when corticosteroids are used. Moreover, corticosteroids may affect the nitroblue-tetrazolium test for bacterial infection and produce false negative results. In cerebral malaria, a double-blind trial has shown that the use of corticosteroids is associated with prolongation of coma and a higher incidence of pneumonia and gastrointestinal bleeding. Corticosteroids may activate latent amebiasis. Therefore, it is recommended that latent or active amebiasis be ruled out before initiating corticosteroid therapy in any patient who has spent time in the tropics or any patient with unexplained diarrhea. Prolonged use of corticosteroids may produce posterior subcapsular cataracts, glaucoma with possible damage to the optic nerves, and may enhance the establishment of secondary ocular infections due to fungi or viruses.
Average and large doses of cortisone or hydrocortisone can cause elevation of blood pressure, salt and water retention, and increased excretion of potassium. These effects are less likely to occur with the synthetic derivatives except when used in large doses. Dietary salt restriction and potassium supplementation may be necessary. All corticosteroids increase calcium excretion. Administration of live virus vaccines, including smallpox, is contraindicated in individuals receiving immunosuppressive doses of corticosteroids. If inactivated viral or bacterial vaccines are administered to individuals receiving immunosuppressive doses of corticosteroids, the expected serum antibody response may not be obtained. However, immunization procedures may be undertaken in patients who are receiving corticosteroids as replacement therapy, e.g., for Addison's disease. Persons who are on drugs which suppress the immune system are more susceptible to infections than healthy individuals. Chickenpox and measles, for example, can have a more serious or even fatal course in non-immune children or adults on corticosteroids. In such children or adults who have not had these diseases, particular care should be taken to avoid exposure. How the dose, route and duration of corticosteroid administration affects the risk of developing a disseminated infection is not known. The contribution of the underlying disease and/or prior corticosteroid treatment to the risk is also not known. If exposed to chickenpox, prophylaxis with varicella zoster immune globulin (VZIG) may be indicated. If exposed to measles, prophylaxis with pooled intramuscular immunoglobulin (IG) may be indicated. (See the respective package inserts for complete VZIG and IG prescribing information). If chickenpox develops, treatment with antiviral agents may be considered.
The use of Dexamethasone Sodium Phosphate Injection, USP in active tuberculosis should be restricted to those cases of fulminating or disseminated tuberculosis in which the corticosteroid is used for the management of the disease in conjunction with an appropriate antituberculous regimen. If corticosteroids are indicated in patients with latent tuberculosis or tuberculin reactivity, close observation is necessary as reactivation of the disease may occur. During prolonged corticosteroid therapy, these patients should receive chemoprophylaxis. Literature reports suggest an apparent association between use of corticosteroids and left ventricular free wall rupture after a recent myocardial infarction; therefore, therapy with corticosteroids should be used with great caution in these patients.
Usage in pregnancy. Since adequate human reproduction studies have not been done with corticosteroids, use of these drugs in pregnancy or in women of childbearing potential requires that the anticipated benefits be weighed against the possible hazards to the mother and embryo or fetus. Infants born of mothers who have received substantial doses of corticosteroids during pregnancy should be carefully observed for signs of hypoadrenalism. Corticosteroids appear in breast milk and could suppress growth, interfere with endogenous corticosteroid production, or cause other unwanted effects. Mothers taking pharmacologic doses of corticosteroids should be advised not to nurse.

Precautions

General
This product, like many other steroid formulations, is sensitive to heat. Therefore, it should not be autoclaved when it is desirable to sterilize the exterior of the vial. Following prolonged therapy, withdrawal of corticosteroids may result in symptoms of the corticosteroid withdrawal syndrome including fever, myalgia, arthralgia, and malaise. This may occur in patients even without evidence of adrenal insufficiency. There is an enhanced effect of corticosteroids in patients with hypothyroidism and in those with cirrhosis. Corticosteroids should be used cautiously in patients with ocular herpes simplex for fear of corneal perforation. The lowest possible dose of corticosteroid should be used to control the condition under treatment, and when reduction in dosage is possible, the reduction must be gradual. Psychic derangements may appear when corticosteroids are used, ranging from euphoria, insomnia, mood swings, personality changes, and severe depression to frank psychotic manifestations. Also, existing emotional instability or psychotic tendencies may be aggravated by corticosteroids.
Aspirin should be used cautiously in conjunction with corticosteroids in hypoprothrombinemia. Steroids should be used with caution in nonspecific ulcerative colitis, if there is a probability of impending perforation, abscess or other pyogenic infection, also in diverticulitis, fresh intestinal anastomoses, active or latent peptic ulcer, renal insufficiency, hypertension, osteoporosis, and myasthenia gravis. Signs of peritoneal irritation following gastrointestinal perforation in patients receiving large doses of corticosteroids may be minimal or absent. Fat embolism has been reported as a possible complication of hypercortisonism. When large doses are given, some authorities advise that antacids be administered between meals to help to prevent peptic ulcer. Growth and development of infants and children on prolonged corticosteroid therapy should be carefully followed. Steroids may increase or decrease motility and number of spermatozoa in some patients. Phenytoin, phenobarbital, ephedrine, and rifampin may enhance the metabolic clearance of corticosteroids resulting in decreased blood levels and lessened physiologic activity, thus requiring adjustment in corticosteroid dosage. These interactions may interfere with dexamethasone suppression tests which should be interpreted with caution during administration of these drugs. False negative results in the dexamethasone suppression test (DST) in patients being treated with indomethacin have been reported. Thus, results of the DST should be interpreted with caution in these patients. The prothrombin time should be checked frequently in patients who are receiving corticosteroids and coumarin anticoagulants at the same time because of reports that corticosteroids have altered the response to these anticoagulants. Studies have shown that the usual effect produced by adding corticosteroids is inhibition of response to coumarins, although there have been some conflicting reports of potentiation not substantiated by studies. When corticosteroids are administered concomitantly with potassium-depleting diuretics, patients should be observed closely for development of hypokalemia. Intra-articular injection of a corticosteroid may produce systemic as well as local effects. Appropriate examination of any joint fluid present is necessary to exclude a septic process. A marked increase in pain accompanied by local swelling, further restriction of joint motion, fever and malaise is suggestive of septic arthritis. If this complication occurs and the diagnosis of sepsis is confirmed, appropriate antimicrobial therapy should be instituted. Injection of a steroid into an infected site is to be avoided. Corticosteroids should not be injected into unstable joints. Patients should be impressed strongly with the importance of not overusing joints in which symptomatic benefit has been obtained as long as the inflammatory process remains active. Frequent intra-articular injection may result in damage to joint tissues. The slower rate of absorption by intramuscular administration should be recognized.
Information for Patients
Persons who are on immunosuppressant doses of corticosteroids should be warned to avoid exposure to chickenpox or measles. Patients should also be advised that if they are exposed, medical advice should be sought without delay.

Adverse Reactions

Fluid and electrolyte disturbances
    Sodium retention
    Fluid retention
    Congestive heart failure in susceptible patients
    Potassium loss
    Hypokalemic alkalosis
    Hypertension

Musculoskeletal
    Muscle weakness
    Steroid myopathy
    Loss of muscle mass
    Osteoporosis
    Vertebral compression fractures
    Aseptic necrosis of femoral and humeral heads
    Pathologic fracture of long bones
    Tendon rupture

Gastrointestinal
    Peptic ulcer with possible subsequent perforation and hemorrhage
    Perforation of the small and large bowel, particularly in patients with inflammatory bowel disease
    Pancreatitis
    Abdominal distention
    Ulcerative esophagitis

Dermatologic
    Impaired wound healing
    Thin fragile skin
    Petechiae and ecchymoses
    Erythema
    Increased sweating
    May suppress reactions to skin tests
    Burning or tingling, especially in the perineal area (after I.V. injection)
    Other cutaneous reactions, such as allergic dermatitis, urticaria, angioneurotic edema

Neurologic
    Convulsions
    Increased intracranial pressure with papilledema (pseudotumor cerebri) usually after treatment
    Vertigo
    Headache
    Psychic disturbances

Endocrine
    Menstrual irregularities
    Development of cushingoid state
    Suppression of growth in children
    Secondary adrenocortical and pituitary unresponsiveness, particularly in times of stress, as in trauma, surgery, or illness
    Decreased carbohydrate tolerance
    Manifestations of latent diabetes mellitus
    Increased requirements for insulin or oral hypoglycemic agents in diabetics
    Hirsutism

Ophthalmic
    Posterior subcapsular cataracts
    Increased intraocular pressure
    Glaucoma
    Exophthalmos

Metabolic
    Negative nitrogen balance due to protein catabolism

Cardiovascular
    Myocardial rupture following recent myocardial infarction (see WARNINGS).

Other
    Anaphylactoid or hypersensitivity reactions
    Thromboembolism
    Weight gain
    Increased appetite
    Nausea
    Malaise
    Hiccups
    The following additional adverse reactions are related to parenteral corticosteroid therapy:
    Rare instances of blindness associated with intralesional therapy around the face and head
    Hyperpigmentation or hypopigmentation
    Subcutaneous and cutaneous atrophy
    Sterile abscess
    Postinjection flare (following intra-articular use)
    Charcot-like arthropathy

Overdosage

Reports of acute toxicity and/or death following overdosage of glucocorticoids are rare. In the event of overdosage, no specific antidote is available; treatment is supportive and symptomatic.
The oral LD50 of dexamethasone in female mice was 6.5 g/kg. The intravenous LD50 of dexamethasone sodium phosphate in female mice was 794 mg/kg.

Dosage and Administration

Dexamethasone Sodium Phosphate Injection, USP, 4 mg/mL -- For intravenous, intramuscular, intra-articular, intralesional, and soft tissue injection.
Dexamethasone Sodium Phosphate Injection, USP can be given directly from the vial, or it can be added to Sodium Chloride Injection or Dextrose Injection and administered by intravenous drip.
Solutions used for intravenous administration or further dilution of this product should be preservative-free when used in the neonate, especially the premature infant.
When it is mixed with an infusion solution, sterile precautions should be observed. Since infusion solutions generally do not contain preservatives, mixtures should be used within 24 hours.
DOSAGE REQUIREMENTS ARE VARIABLE AND MUST BE INDIVIDUALIZED ON THE BASIS OF THE DISEASE AND THE RESPONSE OF THE PATIENT.

Intravenous and Intramuscular Injection

The initial dosage of Dexamethasone sodium phosphate injection varies from 0.5 to 9 mg a day depending on the disease being treated. In less severe diseases doses lower than 0.5 mg may suffice, while in severe diseases doses higher than 9 mg may be required. The initial dosage should be maintained or adjusted until the patient's response is satisfactory. If a satisfactory clinical response does not occur after a reasonable period of time, discontinue Dexamethasone Sodium Phosphate Injection, USP and transfer the patient to other therapy.
After a favorable initial response, the proper maintenance dosage should be determined by decreasing the initial dosage in small amounts to the lowest dosage that maintains an adequate clinical response. Patients should be observed closely for signs that might require dosage adjustment, including changes in clinical status resulting from remissions or exacerbations of the disease, individual drug responsiveness, and the effect of stress (e.g., surgery, infection, trauma). During stress it may be necessary to increase dosage temporarily. If the drug is to be stopped after more than a few days of treatment, it usually should be withdrawn gradually. When the intravenous route of administration is used, dosage usually should be the same as the oral dosage. In certain overwhelming, acute, life-threatening situations, however, administration in dosages exceeding the usual dosages may be justified and may be in multiples of the oral dosages. The slower rate of absorption by intramuscular administration should be recognized.

Shock
There is a tendency in current medical practice to use high (pharmacologic) doses of corticosteroids for the treatment of unresponsive shock. The following dosages of Dexamethasone sodium phosphate injection have been suggested by various authors:

Author*
Dosage
Cavanagh1
3 mg/kg of body weight per 24 hours by constant intravenous infusion after an initial intravenous injection of 20 mg
Dietzman2
2 to 6 mg/kg of body weight as a single intravenous injection
Frank 3
40 mg initially followed by repeat intravenous injection every 4 to 6 hours while shock persists
Oaks4
40 mg initially followed by repeat intravenous injection every 2 to 6 hours while shock persists
Schumer5
1 mg/kg of body weight as a single intravenous injection
*1. Cavanagh, D.; Singh, K.B.: Endotoxin shock in pregnancy and abortion, in: ``Corticosteroids in the Treatment of Shock##, Schumer, W.; Nyhus, L.M., Editors, Urbana, University of Illinois Press, 1970, pp.86-96.
2. Dietzman, R.H.; Ersek, R.A.; Bloch, J.M.; Lillehei, R. C.: High-output, low-resistance gram-negative septic shock in man, Angiology 20: 691-700. Dec. 1969.
3. Frank, E.: Clinical observations in shock and management (In: Shields, T.F., ed.: Symposium on current concepts and management of shock), J. Maine Med. Ass. 59: 195-200. Oct. 1968.
4. Oaks, W. W.; Cohen, H.E.: Endotoxin shock in the geriatric patient, Geriat. 22: 120-130. Mar. 1967.
5. Schumer, W.; Nyhus, L.M.: Corticosteroid effect on biochemical parameters of human oligemic shock, Arch. Surg. 100: 405-408. Apr. 1970.

Although adverse reactions associated with high dose, short term corticosteroid therapy are uncommon, peptic ulceration may occur.

Administration of high dose corticosteroid therapy should be continued only until the patient's condition has stabilized and usually not longer than 48 to 72 hours.

Cerebral Edema
Dexamethasone Sodium Phosphate Injection, USP is generally administered initially in a dosage of 10 mg intravenously followed by four mg every six hours intramuscularly until the symptoms of cerebral edema subside. Response is usually noted within 12 to 24 hours and dosage may be reduced after two to four days and gradually discontinued over a period of five to seven days. For palliative management of patients with recurrent or inoperable brain tumors, maintenance therapy with two mg two or three times a day may be effective.

Acute Allergic Disorders
In acute, self-limited allergic disorders or acute exacerbations of chronic allergic disorders, the following dosage schedule combining parenteral and oral therapy is suggested:

Dexamethasone Sodium Phosphate Injection, USP, 4 mg/mL: first day, 1 or 2 mL (4 or 8 mg), intramuscularly.

This schedule is designed to ensure adequate therapy during acute episodes, while minimizing the risk of overdosage in chronic cases.

Dexamethasone tablets, 0.75 mg: second and third days, 4 tablets in two divided doses each day; Fourth day, 2 tablets in two divided doses; fifth and sixth days, 1 tablet each day; seventh day, no treatment; eighth day, follow-up visit.

Intra-articular, Intralesional, and Soft Tissue Injection

Intra-articular, intralesional, and soft tissue injections are generally employed when the affected joints or areas are limited to one or two sites. Dosage and frequency of injection varies depending on the condition and the site of injection. The usual dose is from 0.2 to 6 mg. The frequency usually ranges from once every three to five days to once every two to three weeks. Frequent intra-articular injection may result in damage to joint tissues.
Some of the usual single doses are:
Site of Injection
Amount of
Dexamethasone Sodium
phosphate
(mg
Large Joints
(e.g., Knee)
2 to 4
Small Joints
(e.g., Interphalangeal,
Temporomandibular)
0.8 to 1
Bursae
2 to 3
Tendon Sheaths
0.4 to 1
Soft Tissue Infiltration
2 to 6
Ganglia

Dexamethasone Sodium Phosphate Injection, USP is particularly recommended for use in conjunction with one of the less soluble, longer-acting steroids for intra-articular and soft tissue injection.
Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever the solution and container permit.

How Supplied

Dexamethasone Sodium Phosphate Injection, USP 4 mg/mL

NDC 0517-4901-25
1 mL Single Dose Vial
Boxes of 25
NDC 0517-4905-25
5 mL Multiple Dose Vial
Boxes of 25
NDC 0517-4930-25
30 mL Multiple Dose Vial
Boxes of 25
Store at 20° - 25°C (68° - 77°F); excursions permitted to 15° - 30°C (59° - 86°F) (See USP Controlled Room Temperature).
Sensitive to heat - Do not autoclave.
IN4901
Rev. 11/05
MG #10095
AMERICAN
REGENT, INC.
SHIRLEY, NY 11967

Sample Package Label

Label


DEXAMETHASONE SODIUM PHOSPHATE 
dexamethasone sodium phosphate   injection, suspension
Product Information
Product TypeHUMAN PRESCRIPTION DRUGNDC Product Code (Source)52584-930 (0517-4930)
Route of AdministrationINTRAVENOUS, INTRAMUSCULAR, INTRA-ARTICULAR, SOFT TISSUE, INTRALESIONALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Dexamethasone Sodium Phosphate (Dexamethasone) Dexamethasone Sodium Phosphate4 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
No Inactive Ingredients Found
Product Characteristics
Color    Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#NDCPackage DescriptionMultilevel Packaging
152584-930-251 VIAL In 1 BAGcontains a VIAL, MULTI-DOSE
130 mL In 1 VIAL, MULTI-DOSEThis package is contained within the BAG (52584-930-25)

Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA08744007/01/2010

Labeler - General Injectables & Vaccines (108250663)
Revised: 07/2010General Injectables & Vaccines