# Bupropion Hydrochloride (XL)

NDC: 83301-0024
Generic name: Bupropion Hydrochloride
Labeler / Manufacturer: Mullan Pharmaceutical Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20240617

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:"83301-0024"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=83301-0024
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=75b1e027-4c5d-46e5-98ee-033e67bd411c