# Bupropion Hydrochloride XL

NDC: 76420-923
Generic name: Bupropion Hydrochloride
Labeler / Manufacturer: Asclemed USA, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20081126

FDA application: ANDA077715

## 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:"76420-923"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=76420-923
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d1d0872c-5b11-4e13-a401-b122348e0fa7