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Naloxone Hydrochloride

NDC 43598-750 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerDr. Reddy's Laboratories, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA213209
Dosage form / routeINJECTION · INTRAMUSCULAR INTRAVENOUS SUBCUTANEOUS
Active ingredientsNALOXONE HYDROCHLORIDE (1 mg/mL)
Marketing started20200318
Package count2

External sources

Source: openFDA. Public-domain (CC0).