FDA NDC Directory · JSON-LD · Markdown

Naloxone Hydrochloride

NDC 42023-224 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerPar Health USA, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA215964
Dosage form / routeINJECTION · INTRAMUSCULAR INTRAVENOUS SUBCUTANEOUS
Active ingredientsNALOXONE HYDROCHLORIDE (1 mg/mL)
Marketing started20241105
Package count1

External sources

Source: openFDA. Public-domain (CC0).