# Bupropion Hydrochloride SR

NDC: 68071-2890
Generic name: bupropion hydrochloride
Labeler / Manufacturer: NuCare Pharmaceuticals,Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20180420

FDA application: ANDA205794

## Active ingredients

- BUPROPION HYDROCHLORIDE: 150 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68071-2890"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68071-2890
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=eeb3fed1-2202-09fc-e053-2995a90a9f63