"68382-194-06" National Drug Code (NDC)

Candesartan Cilexetil And Hydrochlorothiazide 30 TABLET in 1 BOTTLE (68382-194-06)
(Zydus Pharmaceuticals USA Inc.)

NDC Code68382-194-06
Package Description30 TABLET in 1 BOTTLE (68382-194-06)
Product NDC68382-194
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCandesartan Cilexetil And Hydrochlorothiazide
Non-Proprietary NameCandesartan Cilexetil And Hydrochlorothiazide
Dosage FormTABLET
UsageORAL
Start Marketing Date20180414
Marketing Category NameANDA
Application NumberANDA203466
ManufacturerZydus Pharmaceuticals USA Inc.
Substance NameCANDESARTAN CILEXETIL; HYDROCHLOROTHIAZIDE
Strength16; 12.5
Strength Unitmg/1; mg/1
Pharmacy ClassesAngiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]

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