"67253-820-55" National Drug Code (NDC)

Hydrochlorothiazide 5000 TABLET in 1 BOTTLE (67253-820-55)
(DAVA Pharmaceuticals, Inc.)

NDC Code67253-820-55
Package Description5000 TABLET in 1 BOTTLE (67253-820-55)
Product NDC67253-820
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameHydrochlorothiazide
Non-Proprietary NameHydrochlorothiazide
Dosage FormTABLET
UsageORAL
Start Marketing Date19801105
Marketing Category NameANDA
Application NumberANDA087059
ManufacturerDAVA Pharmaceuticals, Inc.
Substance NameHYDROCHLOROTHIAZIDE
Strength25
Strength Unitmg/1
Pharmacy ClassesIncreased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient]

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