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Carvedilol Phosphate

NDC 57664-665 · HUMAN PRESCRIPTION DRUG · CAPSULE, EXTENDED RELEASE

Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA090132
Dosage form / routeCAPSULE, EXTENDED RELEASE · ORAL
Active ingredientsCARVEDILOL PHOSPHATE (40 mg/1)
Marketing started20171108
Package count1

External sources

Source: openFDA. Public-domain (CC0).