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"70518-0123-0" National Drug Code (NDC)

Carvedilol 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0123-0)
(REMEDYREPACK INC.)

NDC Code70518-0123-0
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0123-0)
Product NDC70518-0123
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCarvedilol
Non-Proprietary NameCarvedilol
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20170113
Marketing Category NameANDA
Application NumberANDA078332
ManufacturerREMEDYREPACK 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]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-0123-0





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