# Bupropion Hydrochloride (XL)

NDC: 69097-876
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: 20160829

FDA application: ANDA206556

## 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:"69097-876"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69097-876
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c2cf79d7-1aba-4391-980b-5e218781f7c6