# Bupropion Hydrochloride XL

NDC: 71205-394
Generic name: bupropion hydrochloride
Labeler / Manufacturer: Proficient Rx LP
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20181201

FDA application: ANDA210015

## Active ingredients

- BUPROPION HYDROCHLORIDE: 150 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71205-394"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71205-394
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4a2be6af-e256-4fa9-bfa9-5300d52cdaf4