# Bupropion Hydrochloride

NDC: 47335-954
Generic name: Bupropion Hydrochloride
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20141225

FDA application: ANDA200695

## Active ingredients

- BUPROPION HYDROCHLORIDE: 150 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"47335-954"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=47335-954
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e4e38abf-ef67-405b-af2d-3d8e4533654d