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"67253-821-11" National Drug Code (NDC)

Hydrochlorothiazide 1000 TABLET in 1 BOTTLE (67253-821-11)
(DAVA Pharmaceuticals, Inc.)

NDC Code67253-821-11
Package Description1000 TABLET in 1 BOTTLE (67253-821-11)
Product NDC67253-821
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameHydrochlorothiazide
Non-Proprietary NameHydrochlorothiazide
Dosage FormTABLET
UsageORAL
Start Marketing Date19801105
Marketing Category NameANDA
Application NumberANDA087068
ManufacturerDAVA Pharmaceuticals, Inc.
Substance NameHYDROCHLOROTHIAZIDE
Strength50
Strength Unitmg/1
Pharmacy ClassesIncreased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/67253-821-11





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