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Candesartan cilexetil - 0781-5939-05 - (Candesartan cilexetil)

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Drug Information of Candesartan cilexetil

Product NDC: 0781-5939
Proprietary Name: Candesartan cilexetil
Non Proprietary Name: Candesartan cilexetil
Active Ingredient(s): 32    mg/1 & nbsp;   Candesartan cilexetil
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Candesartan cilexetil

Product NDC: 0781-5939
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078702
Marketing Category: ANDA
Start Marketing Date: 20130521

Package Information of Candesartan cilexetil

Package NDC: 0781-5939-05
Package Description: 500 TABLET in 1 BOTTLE (0781-5939-05)

NDC Information of Candesartan cilexetil

NDC Code 0781-5939-05
Proprietary Name Candesartan cilexetil
Package Description 500 TABLET in 1 BOTTLE (0781-5939-05)
Product NDC 0781-5939
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Candesartan cilexetil
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130521
Marketing Category Name ANDA
Labeler Name Sandoz Inc
Substance Name CANDESARTAN CILEXETIL
Strength Number 32
Strength Unit mg/1
Pharmaceutical Classes Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]

Complete Information of Candesartan cilexetil


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