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NALOXONE HYDROCHLORIDE

NDC 45802-578 · HUMAN OTC DRUG · SPRAY

Generic namenaloxone hydrochloride
Labeler / ManufacturerPadagis Israel Pharmaceuticals Ltd
Marketing categoryAbbreviated NDA (generic) · App ANDA211951
Dosage form / routeSPRAY · NASAL
Active ingredientsNALOXONE HYDROCHLORIDE (4 mg/.1mL)
Marketing started20230730
Package count2

External sources

Source: openFDA. Public-domain (CC0).