FDA NDC Directory · JSON-LD · Markdown

NALOXONE HYDROCHLORIDE

NDC 71205-707 · HUMAN PRESCRIPTION DRUG · SPRAY

Generic namenaloxone hydrochloride
Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA211951
Dosage form / routeSPRAY · NASAL
Active ingredientsNALOXONE HYDROCHLORIDE (4 mg/.1mL)
Marketing started20220621
Package count1

External sources

Source: openFDA. Public-domain (CC0).