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"68788-7603-3" National Drug Code (NDC)

Carvedilol 30 TABLET, FILM COATED in 1 BOTTLE (68788-7603-3)
(Preferred Pharmaceuticals Inc.)

NDC Code68788-7603-3
Package Description30 TABLET, FILM COATED in 1 BOTTLE (68788-7603-3)
Product NDC68788-7603
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCarvedilol
Non-Proprietary NameCarvedilol
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20200207
Marketing Category NameANDA
Application NumberANDA078251
ManufacturerPreferred Pharmaceuticals Inc.
Substance NameCARVEDILOL
Strength6.25
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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