"58118-0162-8" National Drug Code (NDC)

NDC Code	58118-0162-8
Package Description	30 TABLET, FILM COATED in 1 BLISTER PACK (58118-0162-8)
Product NDC	58118-0162
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Carvedilol
Non-Proprietary Name	Carvedilol
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20070905
End Marketing Date	20181201
Marketing Category Name	ANDA
Application Number	ANDA078251
Manufacturer	Clinical Solutions Wholesale
Substance Name	CARVEDILOL
Strength	3.125
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]