"0093-5214-01" National Drug Code (NDC)

Moexipril Hydrochloride And Hydrochlorothiazide 100 TABLET, FILM COATED in 1 BOTTLE (0093-5214-01)
(Teva Pharmaceuticals USA, Inc.)

NDC Code0093-5214-01
Package Description100 TABLET, FILM COATED in 1 BOTTLE (0093-5214-01)
Product NDC0093-5214
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMoexipril Hydrochloride And Hydrochlorothiazide
Non-Proprietary NameMoexipril Hydrochloride And Hydrochlorothiazide
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20070307
End Marketing Date20191130
Marketing Category NameANDA
Application NumberANDA076980
ManufacturerTeva Pharmaceuticals USA, Inc.
Substance NameMOEXIPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE
Strength15; 12.5
Strength Unitmg/1; mg/1
Pharmacy ClassesAngiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS]

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