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NALOXONE HYDROCHLORIDE

NDC 0404-9923 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Generic namenaloxone hydrochloride
Labeler / ManufacturerHenry Schein, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA207633
Dosage form / routeINJECTION, SOLUTION · INTRAMUSCULAR INTRAVENOUS SUBCUTANEOUS
Active ingredientsNALOXONE HYDROCHLORIDE (.4 mg/mL)
Marketing started20220113
Marketing ended20260731
Package count1

External sources

Source: openFDA. Public-domain (CC0).