Label: VETRIPEN G- penicillin g procaine injection, suspension
- NDC Code(s): 13985-522-02, 13985-522-04, 13985-522-05
- Packager: VetOne
- Category: OTC ANIMAL DRUG LABEL
- DEA Schedule: None
- Marketing Status: New Animal Drug Application
Updated February 3, 2020
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(penicillin G procaine)
Injectable antibiotic in aquueous suspension for Cattle, Swine, Sheep, and Horses.
300,000 Units per mL
Sterile, Multiple Dose Vial
NADA 065-505, Approved by FDA
NOT FOR USE IN HUMANS • KEEP OUT OF REACH OF CHILDREN
Penicillin G Procaine Injectable Suspension Alternative Method is available in 100-mL, 250-mL and 500-mL multiple-dose vials. Each mL contains: Active Ingredients: Penicillin G Procaine 300,000 units*, Procaine hydrochloride 130.8 mg*. Inactive Ingredients: Methylparaben 1.3 mg, Propylparaben 0.2 mg, Sodium citrate 10 mg, Sodium carboxymethylcellulose 1 mg, Povidone 5 mg, Lecithin 6 mg, Sodium formaldehyde sulfoxylate 0.2 mg, Procaine hydrochloride 20 mg, and Water for injection, q.s.
*Penicillin G Potassium and Procaine Hydrochloride react to form Penicillin G Procaine.
- MECHANISM OF ACTION
- INDICATIONS & USAGE
DOSAGE & ADMINISTRATION
DIRECTIONS FOR USE: The suspension should be administered by deep intramuscular injection within the fleshy muscles of the hip, rump, round or thigh, or into the neck, changing the site for each injection. Do not inject subcutaneously, into a blood vessel, or near a major nerve. Use a 16 or 18 gauge needle, 1.5 inches long. The needle and syringe should be washed thoroughly before use. The needle and syringe should then be sterilized by placing in boiling water for 15 to 20 minutes. Use this product within 28 days of the first puncture and puncture a maximum of 15 times. Consider using automatic injection equipment or a repeater syringe if necessary to avoid exceeding 15 punctures. When using a draw-off spike or needle with bore diameter larger than 16 gauge, discard any product remaining in the vial immediately after use.
The injection site should be washed with soap and water and painted with a germicide such as tincture of iodine or 70% alcohol. The product should then be administered by using the following procedure:
1. Warm the vial to room temperature and shake thoroughly to ensure uniform suspension.
2. Wipe the rubber stopper on top of the vial with a piece of absorbent cotton soaked in 70% alcohol.
3. Inject air into the vial for easier withdrawal.
4. After filling the syringe, make sure the needle is empty by pulling back the plunger of the syringe until a small air bubble appears. Then detach the needle from the syringe.
5. Insert the needle deep into the muscle, attach the syringe and withdraw the plunger slightly. If blood appears, withdraw the needle and insert it into a different location.
6. Inject the dose slowly. Do not massage the site of injection.
7. Not more than 10 mL should be injected into one location.
Daily treatment should be continued for at least 48 hours after temperature has returned to normal and all other signs of infection have subsided. Animals treated with VetriPen™ G should show noticeable improvement within 36 to 48 hours.
DOSAGE: The dosage for cattle, sheep, swine, and horses is 3000 units per pound of bodyweight, or 1.0 mL for each 100 pounds of bodyweight, once daily. Treatment should not exceed 7 days in non-lactating dairy and beef cattle, sheep, and swine, or 5 days in lactating dairy cattle. If no improvement is observed within 48 hours, consult your veterinarian.
1. Not for use in horses intended for food.
2. Milk that has been taken from animals during treatment and for 48 hours after the last treatment must not be used for food. The daily treatment schedule should not exceed seven (7) days of treatment in non-lactating dairy and beef cattle, sheep and swine, or five (5) days in lactating dairy cattle.
3. The drug should be discontinued for the following time periods before treated animals are slaughtered for food: Cattle - 4 days; Sheep - 8 days; Swine - 6 days; non-ruminating calves - 7 days.
PRECAUTIONS: Sensitivity reactions to penicillin and procaine, such as hives or respiratory distress, may occur in some animals. If such signs of sensitivity occur, stop medication and call your veterinarian. In some instances, particularly if respiratory distress is severe, immediate injection of epinephrine or antihistamine may be necessary. As with any antibiotic preparation, prolonged use may result in overgrowth of non-susceptible organisms, including fungi. If this condition is suspected, stop medication and consult your veterinarian.
- HOW SUPPLIED
- STORAGE AND HANDLING
- GENERAL PRECAUTIONS
- PRINCIPAL DISPLAY PANEL
INGREDIENTS AND APPEARANCE
penicillin g procaine injection, suspension
Product Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:13985-522 Route of Administration INTRAMUSCULAR Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PENICILLIN G PROCAINE (UNII: 17R794ESYN) (PENICILLIN G - UNII:Q42T66VG0C) PENICILLIN G 300000 [USP'U] in 1 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:13985-522-02 100 mL in 1 VIAL, MULTI-DOSE 2 NDC:13985-522-05 500 mL in 1 VIAL, MULTI-DOSE 3 NDC:13985-522-04 250 mL in 1 VIAL, MULTI-DOSE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date NADA NADA065505 08/09/2006 Labeler - VetOne (019926120) Registrant - Bimeda, Inc. (060492923) Establishment Name Address ID/FEI Business Operations Constant Irwindale 010569463 manufacture