# bupropion Hydrochloride

NDC: 72789-544
Generic name: bupropion Hydrochloride
Labeler / Manufacturer: PD-Rx Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20160819

FDA application: ANDA206975

## 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:"72789-544"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72789-544
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=90cc4f07-e0a3-4d50-a10a-8f6a7f9c5140