# Bupropion Hydrochloride SR

NDC: 77771-176
Generic name: bupropion hydrochloride
Labeler / Manufacturer: Radha Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20210415

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:"77771-176"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=77771-176
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=161637d2-bc9d-4a2b-ad1f-6cc39ffd69ce