# Buprenorphine and Naloxone

NDC: 43598-581
Generic name: Buprenorphine and Naloxone
Labeler / Manufacturer: Dr.Reddys Laboratories Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: FILM, SOLUBLE
Routes: BUCCAL, SUBLINGUAL
Marketing started: 20180614

FDA application: ANDA205806

## Active ingredients

- BUPRENORPHINE HYDROCHLORIDE: 12 mg/1
- NALOXONE: 3 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"43598-581"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43598-581
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=72dc1ec0-7c59-a587-4ffd-c40ef79e6fb2