FDA NDC Directory · JSON-LD · Markdown

Valproate Sodium

NDC 25021-797 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerSagent Pharmaceuticals
Marketing categoryAbbreviated NDA (generic) · App ANDA076295
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsVALPROATE SODIUM (100 mg/mL)
Marketing started20241201
Package count1

External sources

Source: openFDA. Public-domain (CC0).