# Bupropion HCL ER(SR)

NDC: 72189-676
Generic name: Bupropion HCL ER(SR)
Labeler / Manufacturer: DriectRx
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20260430

FDA application: ANDA216800

## 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:"72189-676"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72189-676
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=50afb442-e7c6-d28c-e063-6294a90a2b7e