FDA NDC Directory · JSON-LD · Markdown

Valproate Sodium

NDC 63323-494 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Generic nameVALPROATE SODIUM
Labeler / ManufacturerFresenius Kabi USA, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA076539
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsVALPROATE SODIUM (100 mg/mL)
Marketing started20030818
Package count1

External sources

Source: openFDA. Public-domain (CC0).