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Fosphenytoin Sodium

NDC 0641-6136 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerHikma Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA077989
Dosage form / routeINJECTION · INTRAMUSCULAR INTRAVENOUS
Active ingredientsFOSPHENYTOIN SODIUM (50 mg/mL)
Marketing started20070806
Package count1

External sources

Source: openFDA. Public-domain (CC0).