# Buprenorphine

NDC: 0904-7155
Generic name: Buprenorphine
Labeler / Manufacturer: Major Pharmaceuticals
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: SUBLINGUAL
Marketing started: 20091008

FDA application: ANDA078633

## Active ingredients

- BUPRENORPHINE HYDROCHLORIDE: 8 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0904-7155"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0904-7155
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=dba586f9-e3f2-4b9c-849b-907c81a5a0ef