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"71335-2101-5" National Drug Code (NDC)

Carvedilol 90 TABLET, FILM COATED in 1 BOTTLE (71335-2101-5)
(Bryant Ranch Prepack)

NDC Code71335-2101-5
Package Description90 TABLET, FILM COATED in 1 BOTTLE (71335-2101-5)
Product NDC71335-2101
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCarvedilol
Non-Proprietary NameCarvedilol
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20070905
Marketing Category NameANDA
Application NumberANDA077614
ManufacturerBryant Ranch Prepack
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]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/71335-2101-5





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