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Naloxone Hydrochloride

NDC 60219-2104 · HUMAN OTC DRUG · SPRAY

Generic nameNaloxone
Labeler / ManufacturerAmneal Pharmaceuticals NY LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA217992
Dosage form / routeSPRAY · NASAL
Active ingredientsNALOXONE HYDROCHLORIDE (4 mg/.1mL)
Marketing started20240424
Package count1

External sources

Source: openFDA. Public-domain (CC0).