Banamine Injectable Solution Ingredients
(per mL): flunixin meglumine equivalent
to 50 mg flunixin, 0.1 mg edetate disodium, 2.5 mg sodium formaldehyde
sulfoxylate, 4.0 mg diethanolamine, 207.2 mg propylene glycol; 5.0 mg
phenol as preservative, hydrochloric acid, water for injection qs.
Banamine Paste Active Ingredient
(per 30-gm syringe): flunixin meglumine equivalent
to 1500 mg flunixin.
Warnings:
Keep Banamine out of reach of children and animals.
Do not use or store in or near open flame or heat.
Banamine is only intended for use in the animal for
which it was prescribed. Banamine Injectable Solution is for use in
horses and cattle only. Banamine Paste is for use in horses only. Do
not administer to other animals. Not for use in humans.
Follow the dosing and other usage instructions of
your veterinarian's prescription
Caution: Side effects may include localized
swelling, sweating, induration, or stiffness. Rarely, fatal or nonfatal
clostridial infections or other infections occur. Irritation may occur
following injection.
Infection may result at the site of injection. Monitor
site for signs and consult your veterinarian if signs manifest.
Do not use this medication in animals with a known
allergy to it or to similar medications. Seek emergency veterinary treatment
for a hypersensitive reaction.
Seek emergency veterinary attention for a known or
suspected overdose.
Not for use in horses intended for human consumption.
Not for use in dry dairy cows or veal calves.
Do not use within 4 days of slaughter in cattle intended
for consumption. Do not use milk taken during or within 36 hours after
treatment for food.
Do not administer to animals taking another NSAID
or steroid medication.
Avoid intra-arterial injection.
Duration of treatment with this medication should
not exceed 5 consecutive days in horses or 3 consecutive days in cattle.
Do not administer other drugs or supplements concomitantly
with Banamine unless your veterinarian has approved the combination.
Tell your veterinarian if the animal is pregnant,
nursing, or intended for breeding.
This class of NSAID may cause gastrointestinal or
renal toxicity.
Warranty and Manufacturer Information:
Banamine Injectable:
Schering-Plough Animal Health Corp., Union, NJ 07083
Made in Germany
Copyright © (1985, 2003)
Schering-Plough Animal Health Corp. All rights reserved.
NADA #101-479, Approved by FDA.
F-27050603
B-27050603
USA051903INV
US 3029/1
NAC No.: 10470183
Banamine Oral Paste:
U.S. Patent Nos. 5,484,931 and 5,965,735.
NADA #137-409, Approved by FDA.
Made in Ireland.
Copyright © 1985, 1988, 1990, Schering-Plough Animal
Health Corp., Union, NJ 07083. All rights reserved.
NAC No.: 10470192