"42708-079-30" National Drug Code (NDC)

Hydrochlorothiazide 30 TABLET in 1 BOTTLE (42708-079-30)
(QPharma Inc)

NDC Code42708-079-30
Package Description30 TABLET in 1 BOTTLE (42708-079-30)
Product NDC42708-079
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameHydrochlorothiazide
Non-Proprietary NameHydrochlorothiazide
Dosage FormTABLET
UsageORAL
Start Marketing Date20080815
Marketing Category NameANDA
Application NumberANDA040907
ManufacturerQPharma Inc
Substance NameHYDROCHLOROTHIAZIDE
Strength25
Strength Unitmg/1
Pharmacy ClassesIncreased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]

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