SODIUM ASCORBATE injection

SODIUM ASCORBATE by

Drug Labeling and Warnings

SODIUM ASCORBATE by is a Animal medication manufactured, distributed, or labeled by Neogen Corporation - Nandino. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

INDICATIONS & USAGE

INJECTABLE SOLUTION

CAUTION: Federal law restricts this drug to use by or on the order of a licensed veterinarian.

FOR ANIMAL USE ONLY

KEEP OUT OF REACH OF CHILDREN

INDICATIONS

For use as a nutritive supplement of vitamin C in cattle, horses, sheep, swine, dogs and cats.

PRECAUTIONS

Since pressure may develop on long storage, precautions should be taken to release pressure before use. Storage under refrigeration will reduce possibility of pressure build-up.

DOSAGE AND ADMINISTRATION

Administer intramuscularly 1 to 10 mL, depending on condition, species, and body weight. Repeat daily or as indicated by desired response.

TAKE TIME OBSERVE LABEL DIRECTIONS

COMPOSITION

Each mL of sterile aqueous solution contains:

Sodium Ascorbate  . . . . . . . . . . .  250 mg

Monothioglycerol  . . . . . . . . . . .  0.5% w/v

Edetate Disodium   . . . . . . . . . .  0.1% w/v

Methylparaben (preservative) . .  0.18% w/v

Propylparaben (preservative) . .  0.02% w/v

STORAGE AND HANDLING

Store at 20ºC to 25ºC (68º to 77ºF), brief excursions permitted between 15ºC and 30ºC (between 59ºF and 86ºF).
Protect from light.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SODIUM ASCORBATE 
sodium ascorbate injection

Product Information
Product Type	PRESCRIPTION ANIMAL DRUG	Item Code (Source)	NDC: 59051-9077
Route of Administration	INTRAMUSCULAR

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM ASCORBATE (UNII: S033EH8359) (ASCORBIC ACID - UNII:PQ6CK8PD0R)	ASCORBIC ACID	250 mg  in 1 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 59051-9077-5	100 mL in 1 VIAL

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		04/10/2007

Labeler - Neogen Corporation - Nandino (042125879)