# WELLBUTRIN XL

NDC: 0187-0731
Generic name: bupropion hydrochloride
Labeler / Manufacturer: Bausch Health US LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20030829

FDA application: NDA021515

## 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:"0187-0731"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0187-0731
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a435da9d-f6e8-4ddc-897d-8cd2bf777b21