FDA NDC Directory · JSON-LD · Markdown

NALOXONE HYDROCHLORIDE

NDC 55150-328 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerEugia US LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA212456
Dosage form / routeINJECTION, SOLUTION · INTRAMUSCULAR INTRAVENOUS SUBCUTANEOUS
Active ingredientsNALOXONE HYDROCHLORIDE (.4 mg/mL)
Marketing started20191104
Package count2

External sources

Source: openFDA. Public-domain (CC0).