FDA NDC Directory · JSON-LD · Markdown

NALOXONE HYDROCHLORIDE

NDC 51662-1239 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerHF Acquisition Co. LLC, DBA HealthFirst
Marketing categoryAbbreviated NDA (generic) · App ANDA072076
Dosage form / routeINJECTION · PARENTERAL
Active ingredientsNALOXONE HYDROCHLORIDE (1 mg/mL)
Marketing started20180903
Package count2

External sources

Source: openFDA. Public-domain (CC0).