# Bupropion Hydrochloride (XL)

NDC: 68788-4172
Generic name: bupropion hydrochloride
Labeler / Manufacturer: Preferred Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20260724

FDA application: ANDA207479

## 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:"68788-4172"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68788-4172
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=30c370c2-f2b7-4335-ba55-e8c8f4059092