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Naloxone Hydrochloride

NDC 76420-867 · HUMAN OTC DRUG · SPRAY, METERED

Labeler / ManufacturerAsclemed USA, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA209522
Dosage form / routeSPRAY, METERED · NASAL
Active ingredientsNALOXONE HYDROCHLORIDE (4 mg/.1mL)
Marketing started20240923
Package count1

External sources

Source: openFDA. Public-domain (CC0).