FDA NDC Directory · JSON-LD · Markdown

Naloxone Hydrochloride

NDC 76329-3369 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerInternational Medication Systems, Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA072076
Dosage form / routeINJECTION · PARENTERAL
Active ingredientsNALOXONE HYDROCHLORIDE (1 mg/mL)
Marketing started20010601
Package count1

External sources

Source: openFDA. Public-domain (CC0).