FDA NDC Directory · JSON-LD · Markdown

Phenytoin Sodium

NDC 82804-269 · HUMAN PRESCRIPTION DRUG · CAPSULE, EXTENDED RELEASE

Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA040684
Dosage form / routeCAPSULE, EXTENDED RELEASE · ORAL
Active ingredientsPHENYTOIN SODIUM (100 mg/1)
Marketing started20060905
Package count1

External sources

Source: openFDA. Public-domain (CC0).