# BUPROPION HYDROCHLORIDE (SR)

NDC: 69097-879
Generic name: Bupropion Hydrochloride
Labeler / Manufacturer: Cipla USA Inc.,
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20160725

FDA application: ANDA206674

## Active ingredients

- BUPROPION HYDROCHLORIDE: 200 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"69097-879"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69097-879
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9d2c209b-248e-4e26-9cde-fe0abe4428c1