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Fosphenytoin sodium

NDC 68462-945 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerGLENMARK PHARMACEUTICALS INC., USA
Marketing categoryAbbreviated NDA (generic) · App ANDA214926
Dosage form / routeINJECTION, SOLUTION · INTRAMUSCULAR INTRAVENOUS
Active ingredientsFOSPHENYTOIN SODIUM (50 mg/mL)
Marketing started20250528
Package count1

External sources

Source: openFDA. Public-domain (CC0).