"60505-0272-1" National Drug Code (NDC)

Moexipril Hydrochloride 100 TABLET in 1 BOTTLE (60505-0272-1)
(Apotex Corp.)

NDC Code60505-0272-1
Package Description100 TABLET in 1 BOTTLE (60505-0272-1)
Product NDC60505-0272
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMoexipril Hydrochloride
Non-Proprietary NameMoexipril Hydrochloride
Dosage FormTABLET
UsageORAL
Start Marketing Date20080609
Marketing Category NameANDA
Application NumberANDA078454
ManufacturerApotex Corp.
Substance NameMOEXIPRIL HYDROCHLORIDE
Strength15
Strength Unitmg/1
Pharmacy ClassesAngiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]

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