# Bupropion Hydrochloride

NDC: 68001-308
Generic name: Bupropion Hydrochloride
Labeler / Manufacturer: BluePoint Laboratories
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20060117

FDA application: ANDA076143

## Active ingredients

- BUPROPION HYDROCHLORIDE: 75 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68001-308"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68001-308
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7d035056-44ab-444d-9d27-125b3f571140