# BUPROPION HYDROCHLORIDE

NDC: 42571-241
Generic name: Bupropion Hydrochloride
Labeler / Manufacturer: Micro Labs Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20200701

FDA application: ANDA207403

## Active ingredients

- BUPROPION HYDROCHLORIDE: 75 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"42571-241"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42571-241
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=03450d2d-97ce-4518-af15-ab85b0d65d76