"53002-1702-3" National Drug Code (NDC)

Hydrochlorothiazide 30 TABLET in 1 BOTTLE (53002-1702-3)
(RPK Pharmaceuticals, Inc.)

NDC Code53002-1702-3
Package Description30 TABLET in 1 BOTTLE (53002-1702-3)
Product NDC53002-1702
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameHydrochlorothiazide
Non-Proprietary NameHydrochlorothiazide
Dosage FormTABLET
UsageORAL
Start Marketing Date20070312
Marketing Category NameANDA
Application NumberANDA040707
ManufacturerRPK Pharmaceuticals, Inc.
Substance NameHYDROCHLOROTHIAZIDE
Strength12.5
Strength Unitmg/1
Pharmacy ClassesIncreased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]

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