# Carvedilol

NDC: 51655-713
Generic name: Carvedilol
Labeler / Manufacturer: Northwind Health Company, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20210528

FDA application: ANDA078384

## Active ingredients

- CARVEDILOL: 3.125 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51655-713"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51655-713
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=db5d9e64-46b3-92d3-e053-2995a90a74bc