"61786-734-02" National Drug Code (NDC)

Carvedilol 30 TABLET, FILM COATED in 1 BLISTER PACK (61786-734-02)
(REMEDYREPACK INC.)

NDC Code61786-734-02
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (61786-734-02)
Product NDC61786-734
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCarvedilol
Non-Proprietary NameCarvedilol
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20160607
Marketing Category NameANDA
Application NumberANDA076373
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]

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