# Bupropion Hydrochloride

NDC: 70518-1566
Generic name: Bupropion Hydrochloride
Labeler / Manufacturer: REMEDYREPACK INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20181222

FDA application: ANDA076143

## Active ingredients

- BUPROPION HYDROCHLORIDE: 75 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70518-1566"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70518-1566
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3b73d56e-e558-49de-8126-d7ec9b67a086