"51655-002-52" National Drug Code (NDC)

NDC Code	51655-002-52
Package Description	30 TABLET, FILM COATED in 1 BOTTLE, DISPENSING (51655-002-52)
Product NDC	51655-002
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Carvedilol
Non-Proprietary Name	Carvedilol
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20140516
Marketing Category Name	ANDA
Application Number	ANDA077316
Manufacturer	Northwind Pharmaceuticals
Substance Name	CARVEDILOL
Strength	12.5
Strength Unit	mg/301
Pharmacy Classes	Adrenergic alpha-Antagonists [MoA],Adrenergic beta1-Antagonists [MoA],Adrenergic beta2-Antagonists [MoA],alpha-Adrenergic Blocker [EPC],beta-Adrenergic Blocker [EPC]