"70518-0564-0" National Drug Code (NDC)

Carvedilol 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0564-0)
(REMEDYREPACK INC.)

NDC Code70518-0564-0
Package Description180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0564-0)
Product NDC70518-0564
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCarvedilol
Non-Proprietary NameCarvedilol
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20170602
Marketing Category NameANDA
Application NumberANDA078384
ManufacturerREMEDYREPACK INC.
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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