"60505-2938-0" National Drug Code (NDC)

Carvedilol 1 BLISTER PACK in 1 CARTON (60505-2938-0) > 10 TABLET, FILM COATED in 1 BLISTER PACK
(Apotex Corp.)

NDC Code60505-2938-0
Package Description1 BLISTER PACK in 1 CARTON (60505-2938-0) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC60505-2938
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCarvedilol
Non-Proprietary NameCarvedilol
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20070905
Marketing Category NameANDA
Application NumberANDA078165
ManufacturerApotex Corp.
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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