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Valproic Acid

NDC 17856-0152 · HUMAN PRESCRIPTION DRUG · CAPSULE, LIQUID FILLED

Labeler / ManufacturerATLANTIC BIOLOGICALS CORP.
Marketing categoryAbbreviated NDA (generic) · App ANDA073484
Dosage form / routeCAPSULE, LIQUID FILLED · ORAL
Active ingredientsVALPROIC ACID (250 mg/1)
Marketing started20160715
Package count1

External sources

Source: openFDA. Public-domain (CC0).