FDA NDC Directory · JSON-LD · Markdown

Extended Phenytoin Sodium

NDC 65162-212 · HUMAN PRESCRIPTION DRUG · CAPSULE

Generic namePhenytoin Sodium
Labeler / ManufacturerAmneal Pharmaceuticals LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA040765
Dosage form / routeCAPSULE · ORAL
Active ingredientsPHENYTOIN SODIUM (100 mg/1)
Marketing started20091216
Package count4

External sources

Source: openFDA. Public-domain (CC0).