"0093-7295-05" National Drug Code (NDC)

Carvedilol 500 TABLET, FILM COATED in 1 BOTTLE (0093-7295-05)
(Teva Pharmaceuticals USA, Inc.)

NDC Code0093-7295-05
Package Description500 TABLET, FILM COATED in 1 BOTTLE (0093-7295-05)
Product NDC0093-7295
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCarvedilol
Non-Proprietary NameCarvedilol
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20070906
Marketing Category NameANDA
Application NumberANDA076373
ManufacturerTeva Pharmaceuticals USA, Inc.
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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