FDA NDC Directory · JSON-LD · Markdown

NALOXONE HCl

NDC 51662-1620 · HUMAN PRESCRIPTION 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 started20230410
Package count2

External sources

Source: openFDA. Public-domain (CC0).