"42291-222-50" National Drug Code (NDC)

NDC Code	42291-222-50
Package Description	500 TABLET, FILM COATED in 1 BOTTLE (42291-222-50)
Product NDC	42291-222
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Carvedilol
Non-Proprietary Name	Carvedilol
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20120319
Marketing Category Name	ANDA
Application Number	ANDA078332
Manufacturer	AvKARE, Inc.
Substance Name	CARVEDILOL
Strength	6.25
Strength Unit	mg/1
Pharmacy Classes	Adrenergic alpha-Antagonists [MoA],Adrenergic beta1-Antagonists [MoA],Adrenergic beta2-Antagonists [MoA],alpha-Adrenergic Blocker [EPC],beta-Adrenergic Blocker [EPC]