# Carvedilol

NDC: 0781-5224
Generic name: Carvedilol
Labeler / Manufacturer: Sandoz Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20070905
Marketing ended: 20260831
FDA application: ANDA078227

## Active ingredients

- CARVEDILOL: 25 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0781-5224"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0781-5224
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=da8b8c20-0130-4aa9-924d-4a4f28c3f767