# Forfivo XL

NDC: 24979-247
Generic name: bupropion hydrochloride
Labeler / Manufacturer: Upsher-Smith Laboratories, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20231215

FDA application: NDA022497

## Active ingredients

- BUPROPION HYDROCHLORIDE: 450 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"24979-247"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=24979-247
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=80b01182-dc94-4990-8ebb-55c306d7e536