# Buprenorphine

NDC: 60687-481
Generic name: Buprenorphine
Labeler / Manufacturer: American Health Packaging
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: SUBLINGUAL
Marketing started: 20200206

FDA application: ANDA207276

## Active ingredients

- BUPRENORPHINE HYDROCHLORIDE: 2 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"60687-481"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=60687-481
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8d38f7aa-da0b-40ad-b0d1-4284c71042ed