# bupropion hydrochloride SR

NDC: 0904-7465
Generic name: bupropion hydrochloride
Labeler / Manufacturer: Major Pharmaceuticals
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20241115

FDA application: ANDA202304

## 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:"0904-7465"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0904-7465
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=67b6bcf8-0e7c-4e74-ad72-54f1bd6e65ad