"51672-4039-3" National Drug Code (NDC)

Enalapril Maleate 1000 TABLET in 1 BOTTLE (51672-4039-3)
(Taro Pharmaceuticals U.S.A., Inc.)

NDC Code51672-4039-3
Package Description1000 TABLET in 1 BOTTLE (51672-4039-3)
Product NDC51672-4039
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameEnalapril Maleate
Non-Proprietary NameEnalapril Maleate
Dosage FormTABLET
UsageORAL
Start Marketing Date20010123
End Marketing Date20251130
Marketing Category NameANDA
Application NumberANDA075657
ManufacturerTaro Pharmaceuticals U.S.A., Inc.
Substance NameENALAPRIL MALEATE
Strength10
Strength Unitmg/1
Pharmacy ClassesAngiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA], Decreased Blood Pressure [PE]

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