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"71335-1610-0" National Drug Code (NDC)

Hydrochlorothiazide 120 TABLET in 1 BOTTLE (71335-1610-0)
(Bryant Ranch Prepack)

NDC Code71335-1610-0
Package Description120 TABLET in 1 BOTTLE (71335-1610-0)
Product NDC71335-1610
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameHydrochlorothiazide
Non-Proprietary NameHydrochlorothiazide
Dosage FormTABLET
UsageORAL
Start Marketing Date20130410
Marketing Category NameANDA
Application NumberANDA202556
ManufacturerBryant Ranch Prepack
Substance NameHYDROCHLOROTHIAZIDE
Strength25
Strength Unitmg/1
Pharmacy ClassesIncreased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/71335-1610-0





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