# Bupropion Hydrochloride

NDC: 72789-070
Generic name: Bupropion Hydrochloride
Labeler / Manufacturer: PD-Rx Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20060117

FDA application: ANDA076143

## Active ingredients

- BUPROPION HYDROCHLORIDE: 100 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72789-070"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72789-070
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=867d3876-6974-4e89-bc45-9e60e84b401c