FDA NDC Directory · JSON-LD · Markdown

Extended Phenytoin Sodium

NDC 65862-692 · HUMAN PRESCRIPTION DRUG · CAPSULE

Generic namePhenytoin Sodium
Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA204309
Dosage form / routeCAPSULE · ORAL
Active ingredientsPHENYTOIN SODIUM (100 mg/1)
Marketing started20150610
Package count3

External sources

Source: openFDA. Public-domain (CC0).