# Bupropion hydrochloride

NDC: 70518-4081
Generic name: Bupropion hydrochloride
Labeler / Manufacturer: REMEDYREPACK INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20240516

FDA application: ANDA216800

## Active ingredients

- BUPROPION HYDROCHLORIDE: 150 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70518-4081"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70518-4081
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6087100f-3ba4-412e-b08d-768d1dcdaf00