# Bupropion Hydrochloride

NDC: 72241-021
Generic name: Bupropion Hydrochloride
Labeler / Manufacturer: Modavar Pharmaceuticals LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20200116

FDA application: ANDA208606

## Active ingredients

- BUPROPION HYDROCHLORIDE: 100 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72241-021"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72241-021
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0961f83e-25e9-4ffc-8669-44e4e9169978