# Bupropion Hydrochloride XL

NDC: 80425-0468
Generic name: Bupropion Hydrochloride
Labeler / Manufacturer: Advanced Rx of Tennessee, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20250101

FDA application: ANDA207224

## 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:"80425-0468"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=80425-0468
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2aabf040-16a6-b772-e063-6294a90afd70