# Bupropion hydrochloride

NDC: 68788-8769
Generic name: Bupropion hydrochloride
Labeler / Manufacturer: Preferred Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20241119

FDA application: ANDA216800

## 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:"68788-8769"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68788-8769
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=093c4a61-02d9-4b55-b612-569aa25d3f2a