# WELLBUTRIN SR

NDC: 0173-0722
Generic name: bupropion hydrochloride
Labeler / Manufacturer: GlaxoSmithKline LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20020625

FDA application: NDA020358

## 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:"0173-0722"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0173-0722
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=cbc8c074-f080-4489-a5ae-207b5fadeba3