"0555-0483-05" National Drug Code (NDC)

Amiloride Hydrochloride And Hydrochlorothiazide 1000 TABLET in 1 BOTTLE (0555-0483-05)
(Teva Pharmaceuticals USA, Inc.)

NDC Code0555-0483-05
Package Description1000 TABLET in 1 BOTTLE (0555-0483-05)
Product NDC0555-0483
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAmiloride Hydrochloride And Hydrochlorothiazide
Non-Proprietary NameAmiloride Hydrochloride And Hydrochlorothiazide
Dosage FormTABLET
UsageORAL
Start Marketing Date19891201
Marketing Category NameANDA
Application NumberANDA071111
ManufacturerTeva Pharmaceuticals USA, Inc.
Substance NameAMILORIDE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE
Strength5; 50
Strength Unitmg/1; mg/1
Pharmacy ClassesDecreased Renal K+ Excretion [PE], Increased Diuresis [PE], Increased Diuresis [PE], Potassium-sparing Diuretic [EPC], Thiazide Diuretic [EPC], Thiazides [CS]

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