"0574-0110-01" National Drug Code (NDC)

Moexipril Hydrochloride 100 TABLET, COATED in 1 BOTTLE, PLASTIC (0574-0110-01)
(Paddock Laboratories, Inc.)

NDC Code0574-0110-01
Package Description100 TABLET, COATED in 1 BOTTLE, PLASTIC (0574-0110-01)
Product NDC0574-0110
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMoexipril Hydrochloride
Non-Proprietary NameMoexipril Hydrochloride
Dosage FormTABLET, COATED
UsageORAL
Start Marketing Date20061130
Marketing Category NameANDA
Application NumberANDA077536
ManufacturerPaddock Laboratories, Inc.
Substance NameMOEXIPRIL HYDROCHLORIDE
Strength7.5
Strength Unitmg/1
Pharmacy ClassesAngiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]

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