Label: VITAMIN C- sodium ascorbate injection
- NDC Code(s): 57561-348-04, 57561-348-05
- Packager: Agri Laboratories, Ltd.
- Category: PRESCRIPTION ANIMAL DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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.
Drug Label Information
Updated September 28, 2015
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- INDICATIONS & USAGE
- PRECAUTIONS
- DOSAGE AND ADMINISTRATION
- COMPOSITION
- STORAGE AND HANDLING
- VITAMIN C INJECTABLE SOLUTION
-
INGREDIENTS AND APPEARANCE
VITAMIN C
sodium ascorbate injectionProduct Information Product Type PRESCRIPTION ANIMAL DRUG Item Code (Source) NDC:57561-348 Route of Administration INTRAMUSCULAR Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM ASCORBATE (UNII: S033EH8359) (ASCORBIC ACID - UNII:PQ6CK8PD0R) SODIUM ASCORBATE 250 mg in 1 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:57561-348-04 100 mL in 1 VIAL 2 NDC:57561-348-05 250 mL in 1 VIAL Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 07/31/2007 Labeler - Agri Laboratories, Ltd. (155594450)