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Buprenorphine and Naloxone

NDC 43598-581 · HUMAN PRESCRIPTION DRUG · FILM, SOLUBLE

Labeler / ManufacturerDr.Reddys Laboratories Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA205806
Dosage form / routeFILM, SOLUBLE · BUCCAL SUBLINGUAL
Active ingredientsBUPRENORPHINE HYDROCHLORIDE (12 mg/1)
NALOXONE (3 mg/1)
Marketing started20180614
Package count1

External sources

Source: openFDA. Public-domain (CC0).