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Naloxone Hydrochloride

NDC 67457-992 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerMylan Institutional LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA213843
Dosage form / routeINJECTION, SOLUTION · INTRAMUSCULAR INTRAVENOUS SUBCUTANEOUS
Active ingredientsNALOXONE HYDROCHLORIDE (1 mg/mL)
Marketing started20221202
Package count1

External sources

Source: openFDA. Public-domain (CC0).