# Bupropion Hydrochloride

NDC: 63629-2138
Generic name: Bupropion Hydrochloride
Labeler / Manufacturer: Bryant Ranch Prepack
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20070612

FDA application: ANDA077284

## Active ingredients

- BUPROPION HYDROCHLORIDE: 300 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63629-2138"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63629-2138
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=bd3f1706-e6e0-4db1-b09e-5e718976766a