FDA NDC Directory · JSON-LD · Markdown

Dilantin-125

NDC 58151-115 · HUMAN PRESCRIPTION DRUG · SUSPENSION

Generic namePhenytoin
Labeler / ManufacturerViatris Specialty LLC
Marketing categoryNew Drug Application (innovator) · App NDA008762
Dosage form / routeSUSPENSION · ORAL
Active ingredientsPHENYTOIN (125 mg/5mL)
Marketing started20240419
Package count1

External sources

Source: openFDA. Public-domain (CC0).