# BUPROPION HYDROCHLORIDE

NDC: 55700-820
Generic name: BUPROPION HYDROCHLORIDE
Labeler / Manufacturer: Quality Care Products, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20191122
Marketing ended: 20260831
FDA application: ANDA210497

## 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:"55700-820"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=55700-820
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a225dbbb-86f0-4547-a1c8-68eb64cd6892