# Bupropion Hydrochloride SR

NDC: 82868-019
Generic name: bupropion hydrochloride
Labeler / Manufacturer: Northwind Health Company, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20231019

FDA application: ANDA205794

## Active ingredients

- BUPROPION HYDROCHLORIDE: 150 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"82868-019"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=82868-019
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0865f8cf-1d7f-0e67-e063-6294a90a2f4d