# Bupropion Hydrobromide

NDC: 68682-582
Generic name: Bupropion Hydrobromide
Labeler / Manufacturer: Oceanside Pharmaceuticals
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: NDA AUTHORIZED GENERIC
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20260629

FDA application: NDA022108

## Active ingredients

- BUPROPION HYDROBROMIDE: 522 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68682-582"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68682-582
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3ec04240-baef-44d7-8d73-a181171eec43