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naloxone hydrochloride

NDC 43066-142 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerBaxter Healthcare Corporation
Marketing categoryAbbreviated NDA (generic) · App ANDA214785
Dosage form / routeINJECTION, SOLUTION · INTRAMUSCULAR INTRAVENOUS SUBCUTANEOUS
Active ingredientsNALOXONE HYDROCHLORIDE (1 mg/mL)
Marketing started20250603
Package count1

External sources

Source: openFDA. Public-domain (CC0).