# Bupropion Hydrochloride

NDC: 0115-5445
Generic name: BUPROPION HYDROCHLORIDE
Labeler / Manufacturer: Amneal Pharmaceuticals of New York LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20041203

FDA application: ANDA076711

## Active ingredients

- BUPROPION HYDROCHLORIDE: 200 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0115-5445"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0115-5445
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e962fb9a-d9fb-49c5-a8b4-0b355b8f829b