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"70518-0169-2" National Drug Code (NDC)

Carvedilol 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0169-2)
(REMEDYREPACK INC.)

NDC Code70518-0169-2
Package Description90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0169-2)
Product NDC70518-0169
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCarvedilol
Non-Proprietary NameCarvedilol
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20170123
Marketing Category NameANDA
Application NumberANDA078332
ManufacturerREMEDYREPACK INC.
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]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-0169-2





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