"59762-1737-7" National Drug Code (NDC)

Hydrochlorothiazide 1000 TABLET in 1 BOTTLE (59762-1737-7)
(Greenstone LLC)

NDC Code59762-1737-7
Package Description1000 TABLET in 1 BOTTLE (59762-1737-7)
Product NDC59762-1737
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameHydrochlorothiazide
Non-Proprietary NameHydrochlorothiazide
Dosage FormTABLET
UsageORAL
Start Marketing Date20070720
End Marketing Date20140630
Marketing Category NameANDA
Application NumberANDA040780
ManufacturerGreenstone LLC
Substance NameHYDROCHLOROTHIAZIDE
Strength50
Strength Unitmg/1
Pharmacy ClassesIncreased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient]

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