"0172-2083-80" National Drug Code (NDC)

Hydrochlorothiazide 1000 TABLET in 1 BOTTLE (0172-2083-80)
(Teva Pharmaceuticals USA, Inc.)

NDC Code0172-2083-80
Package Description1000 TABLET in 1 BOTTLE (0172-2083-80)
Product NDC0172-2083
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameHydrochlorothiazide
Non-Proprietary NameHydrochlorothiazide
Dosage FormTABLET
UsageORAL
Start Marketing Date19730112
Marketing Category NameANDA
Application NumberANDA083177
ManufacturerTeva Pharmaceuticals USA, Inc.
Substance NameHYDROCHLOROTHIAZIDE
Strength25
Strength Unitmg/1
Pharmacy ClassesIncreased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]

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