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"61919-728-90" National Drug Code (NDC)

Carvedilol 90 TABLET, FILM COATED in 1 BOTTLE (61919-728-90)
(Direct_Rx)

NDC Code61919-728-90
Package Description90 TABLET, FILM COATED in 1 BOTTLE (61919-728-90)
Product NDC61919-728
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCarvedilol
Non-Proprietary NameCarvedilol
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20190115
Marketing Category NameANDA
Application NumberANDA078332
ManufacturerDirect_Rx
Substance NameCARVEDILOL
Strength12.5
Strength Unitmg/1
Pharmacy ClassesAdrenergic alpha-Antagonists [MoA], Adrenergic beta1-Antagonists [MoA], Adrenergic beta2-Antagonists [MoA], alpha-Adrenergic Blocker [EPC], beta-Adrenergic Blocker [EPC]

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