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"68001-151-03" National Drug Code (NDC)

Carvedilol 500 TABLET, FILM COATED in 1 BOTTLE (68001-151-03)
(BluePoint Laboratories)

NDC Code68001-151-03
Package Description500 TABLET, FILM COATED in 1 BOTTLE (68001-151-03)
Product NDC68001-151
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCarvedilol
Non-Proprietary NameCarvedilol
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20140422
Marketing Category NameANDA
Application NumberANDA077614
ManufacturerBluePoint Laboratories
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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