# Bupropion Hydrochloride

NDC: 76420-812
Generic name: Bupropion Hydrochloride
Labeler / Manufacturer: Asclemed USA, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20150217

FDA application: ANDA077285

## Active ingredients

- BUPROPION HYDROCHLORIDE: 300 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"76420-812"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=76420-812
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=637e89e5-8f6e-4392-8045-a778cb9ed138