FDA NDC Directory · JSON-LD · Markdown

NALOXONE HYDROCHLORIDE

NDC 51662-1659 · HUMAN OTC DRUG · SPRAY

Labeler / ManufacturerHF Acquisition Co LLC, DBA HealthFirst
Marketing categoryAbbreviated NDA (generic) · App ANDA211951
Dosage form / routeSPRAY · NASAL
Active ingredientsNALOXONE HYDROCHLORIDE (4 mg/.1mL)
Marketing started20230730
Package count1

External sources

Source: openFDA. Public-domain (CC0).