FDA NDC Directory · JSON-LD · Markdown

NALOXONE HYDROCHLORIDE

NDC 51662-1238 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerHF Acquisition Co. LLC, DBA HealthFirst
Marketing categoryAbbreviated NDA (generic) · App ANDA070172
Dosage form / routeINJECTION, SOLUTION · INTRAMUSCULAR INTRAVENOUS SUBCUTANEOUS
Active ingredientsNALOXONE HYDROCHLORIDE (.4 mg/mL)
Marketing started20180903
Package count1

External sources

Source: openFDA. Public-domain (CC0).