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"55111-253-78" National Drug Code (NDC)

Carvedilol 10 BLISTER PACK in 1 CARTON (55111-253-78) > 10 TABLET, FILM COATED in 1 BLISTER PACK (55111-253-79)
(Dr. Reddy's Laboratories Limited)

NDC Code55111-253-78
Package Description10 BLISTER PACK in 1 CARTON (55111-253-78) > 10 TABLET, FILM COATED in 1 BLISTER PACK (55111-253-79)
Product NDC55111-253
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCarvedilol
Non-Proprietary NameCarvedilol
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20070905
Marketing Category NameANDA
Application NumberANDA076649
ManufacturerDr. Reddy's Laboratories Limited
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]

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