Țară: Statele Unite ale Americii
Limbă: engleză
Sursă: NLM (National Library of Medicine)
SODIUM IODIDE (UNII: F5WR8N145C) (IODIDE ION - UNII:09G4I6V86Q)
AgriLabs
INTRAVENOUS
PRESCRIPTION
For use as an aid in the treatment of actinomycosis (lumpy jaw) actinobacillosis (wooden tongue) and necrotic stomatitis in cattle. The use of sodium iodide is contraindicated in pregnancy and hyperthyroidism. For Animal Use Only
unapproved drug other
SODIUM IODIDE- SODIUM IODIDE INJECTION, SOLUTION AGRILABS _Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been_ _approved by FDA. For further information about unapproved drugs, click here._ ---------- SODIUM IODIDE 20% INJECTION INDICATIONS: For use as an aid in the treatment of actinomycosis (lumpy jaw) actinobacillosis (wooden tongue) and necrotic stomatitis in cattle. CONTRAINDICATIONS: The use of sodium iodide is contraindicated in pregnancy and hyperthyroidism. CAUTION: Animals vary in their suscep- tibility of iodides. Administer with caution until the animal's tolerance is determined. Discontinue treatment if adverse reactions occur. DOSAGE AND ADMINISTRATION: Using aspetic procedures, administer slowly by intravenous injection. Inject carefully to avoid deposition outside of the vein. The usual dose is 30 mg per pound of body weight (15 mL/100 lb). May be repeated at weekly intervals, if necessary. WARNING: Not for use in lactating dairy cows. FOR ANIMAL USE ONLY KEEP OUT OF REACH OF CHILDREN CAUTION: Federal law restricts this drug to use by or on the order of a licensed veterinarian. COMPOSITION: Each 100 mL of sterile aqueous solution contains: Sodium Iodide...................20 grams Water For Injection.................q.s. STORE BETWEEN 15°C AND 30°C (59°F AND 86°F). TAKE TIME OBSERVE LABEL DIRECTIONS ®Registered trademark of Agri Laboratories, Ltd. Iss. 07-10 LOT EXP NDC 57561-614-25 RMS 92-589 18-819-25 MANUFACTURED FOR AGRI LABORATORIES, LTD. ST. JOSEPH, MO 64503 SODIUM IODIDE sodium iodide injection, solution PRODUCT INFORMATION PRODUCT T YPE PRESCRIPTION ANIMAL DRUG ITE M CODE (SOURCE ) NDC:5756 1-6 14 ROUTE OF ADMINISTRATION INTRAVENOUS AgriLabs ACTIVE INGREDIENT/ACTIVE MOIETY INGREDIENT NAME BASIS OF STRENGTH STRE NG TH SO DIUM IO DIDE (UNII: F5WR8 N145C) (IODIDE ION - UNII:0 9 G4I6 V8 6 Q) IODIDE ION 20 g in 10 0 mL PACKAG ING # ITEM CODE PACKAGE DESCRIPTION MARKETING START DATE MARKETING END DATE 1 NDC:5756 1-6 14-25 250 mL in 1 BOTT Citiți documentul complet