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Buprenorphine and Naloxone

NDC 43598-579 · HUMAN PRESCRIPTION DRUG · FILM, SOLUBLE

Labeler / ManufacturerDr.Reddys Laboratories Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA205299
Dosage form / routeFILM, SOLUBLE · BUCCAL SUBLINGUAL
Active ingredientsBUPRENORPHINE HYDROCHLORIDE (2 mg/1)
NALOXONE (.5 mg/1)
Marketing started20180614
Package count1

External sources

Source: openFDA. Public-domain (CC0).