FDA NDC Directory · JSON-LD · Markdown

PHENYTOIN SODIUM

NDC 61919-815 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerDIRECT RX
Marketing categoryAbbreviated NDA (generic) · App ANDA040765
Dosage form / routeCAPSULE · ORAL
Active ingredientsPHENYTOIN SODIUM (100 mg/1)
Marketing started20140101
Package count3

External sources

Source: openFDA. Public-domain (CC0).