FDA NDC Directory · JSON-LD · Markdown

Naloxone Hydrochloride

NDC 0591-3871 · HUMAN OTC DRUG · SPRAY, METERED

Labeler / ManufacturerActavis Pharma, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA209522
Dosage form / routeSPRAY, METERED · NASAL
Active ingredientsNALOXONE HYDROCHLORIDE (4 mg/.1mL)
Marketing started20250117
Package count1

External sources

Source: openFDA. Public-domain (CC0).