# buprenorphine hydrochloride

NDC: 70518-4570
Generic name: buprenorphine hydrochloride
Labeler / Manufacturer: REMEDYREPACK INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: SUBLINGUAL
Marketing started: 20260210

FDA application: ANDA090279

## 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:"70518-4570"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70518-4570
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9f7b0a28-f937-4d4d-b793-ca3468bd28e0