# BUPROPION HYDROCHLORIDE

NDC: 0615-8582
Generic name: BUPROPION HYDROCHLORIDE
Labeler / Manufacturer: NCS HealthCare of KY, LLC dba Vangard Labs
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20240425

FDA application: ANDA075491

## Active ingredients

- BUPROPION HYDROCHLORIDE: 100 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0615-8582"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0615-8582
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4fbe64aa-f8f4-45fa-88ae-e844997703ae