FDA NDC Directory · JSON-LD · Markdown

Phenytoin

NDC 17856-4070 · HUMAN PRESCRIPTION DRUG · SUSPENSION

Labeler / ManufacturerATLANTIC BIOLOGICALS CORP.
Marketing categoryAbbreviated NDA (generic) · App ANDA040521
Dosage form / routeSUSPENSION · ORAL
Active ingredientsPHENYTOIN (125 mg/5mL)
Marketing started20040408
Package count1

External sources

Source: openFDA. Public-domain (CC0).