# Bupropion hydrochloride (XL)

NDC: 69680-157
Generic name: Bupropion hydrochloride
Labeler / Manufacturer: Vitruvias Therapeutics
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20230410

FDA application: ANDA208652

## Active ingredients

- BUPROPION HYDROCHLORIDE: 150 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"69680-157"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69680-157
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f53704b2-3d3c-47e8-9fd6-a0f5240c0593