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"61919-730-90" National Drug Code (NDC)

Carvedilol 90 TABLET, FILM COATED in 1 BOTTLE (61919-730-90)
(DIRECT RX)

NDC Code61919-730-90
Package Description90 TABLET, FILM COATED in 1 BOTTLE (61919-730-90)
Product NDC61919-730
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCarvedilol
Non-Proprietary NameCarvedilol
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20190422
Marketing Category NameANDA
Application NumberANDA078332
ManufacturerDIRECT RX
Substance NameCARVEDILOL
Strength25
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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