# Buprenorphine Hydrochloride

NDC: 0143-9246
Generic name: Buprenorphine Hydrochloride
Labeler / Manufacturer: Hikma Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20050525

FDA application: ANDA076931

## Active ingredients

- BUPRENORPHINE HYDROCHLORIDE: .324 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0143-9246"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0143-9246
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=adc1167e-910e-4d7b-abdc-751d3df0c3dc