FDA NDC Directory · JSON-LD · Markdown

Divalproex sodium

NDC 70518-3457 · HUMAN PRESCRIPTION DRUG · CAPSULE, COATED PELLETS

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA213181
Dosage form / routeCAPSULE, COATED PELLETS · ORAL
Active ingredientsDIVALPROEX SODIUM (125 mg/1)
Marketing started20200720
Package count2

External sources

Source: openFDA. Public-domain (CC0).