"53002-4972-3" National Drug Code (NDC)

Hydrochlorothiazide 30 TABLET in 1 BOTTLE (53002-4972-3)
(RPK Pharmaceuticals, Inc.)

NDC Code53002-4972-3
Package Description30 TABLET in 1 BOTTLE (53002-4972-3)
Product NDC53002-4972
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameHydrochlorothiazide
Non-Proprietary NameHydrochlorothiazide
Dosage FormTABLET
UsageORAL
Start Marketing Date19730112
Marketing Category NameANDA
Application NumberANDA083177
ManufacturerRPK Pharmaceuticals, Inc.
Substance NameHYDROCHLOROTHIAZIDE
Strength25
Strength Unitmg/1
Pharmacy ClassesIncreased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]

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