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"52125-210-02" National Drug Code (NDC)

Carvedilol 30 TABLET, FILM COATED in 1 BLISTER PACK (52125-210-02)
(REMEDYREPACK INC.)

NDC Code52125-210-02
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (52125-210-02)
Product NDC52125-210
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCarvedilol
Non-Proprietary NameCarvedilol
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20120829
Marketing Category NameANDA
Application NumberANDA076373
ManufacturerREMEDYREPACK INC.
Substance NameCARVEDILOL
Strength3.125
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/52125-210-02





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