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Phenytoin Sodium

NDC 29300-379 · HUMAN PRESCRIPTION DRUG · CAPSULE, EXTENDED RELEASE

Labeler / ManufacturerUnichem Pharmaceuticals (USA), Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA213834
Dosage form / routeCAPSULE, EXTENDED RELEASE · ORAL
Active ingredientsPHENYTOIN SODIUM (100 mg/1)
Marketing started20221112
Package count3

External sources

Source: openFDA. Public-domain (CC0).