"68382-416-77" National Drug Code (NDC)

Candesartan Cilexetil And Hydrochlorothiazide 10 BLISTER PACK in 1 CARTON (68382-416-77) > 10 TABLET in 1 BLISTER PACK
(Zydus Pharmaceuticals USA Inc.)

NDC Code68382-416-77
Package Description10 BLISTER PACK in 1 CARTON (68382-416-77) > 10 TABLET in 1 BLISTER PACK
Product NDC68382-416
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; 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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