Ülke: ABD
Dil: İngilizce
Kaynak: NLM (National Library of Medicine)
SODIUM IODIDE (UNII: F5WR8N145C) (IODIDE ION - UNII:09G4I6V86Q)
Nova-Tech, Inc.
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 NOVA-TECH, INC. _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% 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 susceptibility 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-30°C (59°F-86°F). TAKE TIME OBSERVE LABEL DIRECTIONS Manufactured by: Nova-Tech, Inc. Grand Island, NE 68801 USA 18-819 RMS 92-366 NDC# 65207-819-25 Net Contents: 250 mL (8.45 fl oz) Assembled in USA Lot No. Exp. Date SODIUM IODIDE sodium iodide injection, solution PRODUCT INFORMATION PRODUCT T YPE PRESCRIPTION ANIMAL DRUG ITE M CODE (SOURCE ) NDC:6 520 7-8 19 ROUTE OF ADMINISTRATION INTRAVENOUS 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 Nova-Tech, Inc. 1 NDC:6 520 7-8 19 -25 250 mL in 1 BOTTLE, PLASTIC Belgenin tamamını okuyun