# Bupropion Hydrochloride SR

NDC: 43598-538
Generic name: bupropion hydrochloride
Labeler / Manufacturer: Dr. Reddys Laboratories Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20160801

FDA application: ANDA205794

## 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:"43598-538"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43598-538
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6948f63b-599c-4956-a249-e9544beda9fc