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Candesartan Cilexetil-Hydrochlorothiazide - 49884-662-09 - (Candesartan Cilexetil and Hydrochlorothiazide)

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Drug Information of Candesartan Cilexetil-Hydrochlorothiazide

Product NDC: 49884-662
Proprietary Name: Candesartan Cilexetil-Hydrochlorothiazide
Non Proprietary Name: Candesartan Cilexetil and Hydrochlorothiazide
Active Ingredient(s): 16; 12.5    mg/1; mg/1 & nbsp;   Candesartan Cilexetil and Hydrochlorothiazide
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Candesartan Cilexetil-Hydrochlorothiazide

Product NDC: 49884-662
Labeler Name: Par Pharmaceutical Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021093
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20121205

Package Information of Candesartan Cilexetil-Hydrochlorothiazide

Package NDC: 49884-662-09
Package Description: 90 TABLET in 1 BOTTLE (49884-662-09)

NDC Information of Candesartan Cilexetil-Hydrochlorothiazide

NDC Code 49884-662-09
Proprietary Name Candesartan Cilexetil-Hydrochlorothiazide
Package Description 90 TABLET in 1 BOTTLE (49884-662-09)
Product NDC 49884-662
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Candesartan Cilexetil and Hydrochlorothiazide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20121205
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Par Pharmaceutical Inc.
Substance Name CANDESARTAN CILEXETIL; HYDROCHLOROTHIAZIDE
Strength Number 16; 12.5
Strength Unit mg/1; mg/1
Pharmaceutical Classes Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient]

Complete Information of Candesartan Cilexetil-Hydrochlorothiazide


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