FDA NDC Directory · JSON-LD · Markdown

Naloxone Hydrochloride

NDC 0409-1215 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Generic nameNALOXONE HYDROCHLORIDE
Labeler / ManufacturerHospira, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA070256
Dosage form / routeINJECTION, SOLUTION · INTRAMUSCULAR INTRAVENOUS SUBCUTANEOUS
Active ingredientsNALOXONE HYDROCHLORIDE (.4 mg/mL)
Marketing started20050712
Package count1

External sources

Source: openFDA. Public-domain (CC0).