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epinephrine

NDC 68462-933 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION, CONCENTRATE

Labeler / ManufacturerGLENMARK PHARMACEUTICALS INC., USA
Marketing categoryAbbreviated NDA (generic) · App ANDA218144
Dosage form / routeINJECTION, SOLUTION, CONCENTRATE · INTRAMUSCULAR INTRAOCULAR INTRAVENOUS SUBCUTANEOUS
Active ingredientsEPINEPHRINE (1 mg/mL)
Marketing started20250603
Package count1

External sources

Source: openFDA. Public-domain (CC0).