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Folic Acid

NDC 63323-184 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerFresenius Kabi USA, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA089202
Dosage form / routeINJECTION, SOLUTION · INTRAMUSCULAR INTRAVENOUS SUBCUTANEOUS
Active ingredientsFOLIC ACID (5 mg/mL)
Marketing started20000905
Package count1

External sources

Source: openFDA. Public-domain (CC0).