"70771-1327-0" National Drug Code (NDC)

Candesartan Cilexetil And Hydrochlorothiazide 1000 TABLET in 1 BOTTLE (70771-1327-0)
(Zydus Lifesciences Limited)

NDC Code70771-1327-0
Package Description1000 TABLET in 1 BOTTLE (70771-1327-0)
Product NDC70771-1327
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 Lifesciences Limited
Substance NameCANDESARTAN CILEXETIL; HYDROCHLOROTHIAZIDE
Strength32; 25
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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