"68788-9738-3" National Drug Code (NDC)

Carvedilol 30 TABLET, FILM COATED in 1 BOTTLE (68788-9738-3)
(Preferred Pharmaceuticals, Inc.)

NDC Code68788-9738-3
Package Description30 TABLET, FILM COATED in 1 BOTTLE (68788-9738-3)
Product NDC68788-9738
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCarvedilol
Non-Proprietary NameCarvedilol
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20130327
Marketing Category NameANDA
Application NumberANDA078332
ManufacturerPreferred Pharmaceuticals, 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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