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Naloxone Hydrochloride Injection, USP, Auto-Injector

NDC 60842-002 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Generic nameNaloxone Hydrochloride
Labeler / ManufacturerKaleo, Inc.
Marketing categoryNew Drug Application (innovator) · App NDA215457
Dosage form / routeINJECTION, SOLUTION · INTRAMUSCULAR SUBCUTANEOUS
Active ingredientsNALOXONE HYDROCHLORIDE (10 mg/.4mL)
Marketing started20220228
Package count1

External sources

Source: openFDA. Public-domain (CC0).