"68382-195-01" National Drug Code (NDC)

Candesartan Cilexetil And Hydrochlorothiazide 100 TABLET in 1 BOTTLE (68382-195-01)
(Zydus Pharmaceuticals USA Inc.)

NDC Code68382-195-01
Package Description100 TABLET in 1 BOTTLE (68382-195-01)
Product NDC68382-195
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
Strength32; 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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