# Bupropion Hydrochloride XL

NDC: 0904-7505
Generic name: Bupropion Hydrochloride
Labeler / Manufacturer: Major Pharmaceuticals
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20241125

FDA application: ANDA090693

## 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:"0904-7505"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0904-7505
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=aa3d3e5b-74a3-47f6-b9aa-d6e248e950e5