# CARVEDILOL

NDC: 68071-3970
Generic name: CARVEDILOL
Labeler / Manufacturer: NuCare Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20210729

FDA application: ANDA078165

## 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:"68071-3970"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68071-3970
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4bbf3767-8666-22d8-e063-6294a90a2afe