SODIUM IODIDE injection, solution

Pays: États-Unis

Langue: anglais

Source: NLM (National Library of Medicine)

Ingrédients actifs:

SODIUM IODIDE (UNII: F5WR8N145C) (IODIDE ION - UNII:09G4I6V86Q)

Disponible depuis:

Nova-Tech, Inc.

Mode d'administration:

INTRAVENOUS

Type d'ordonnance:

PRESCRIPTION

indications thérapeutiques:

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

Statut de autorisation:

unapproved drug other

Résumé des caractéristiques du produit

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._
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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