ATACAND - 0186-0032-54 - (Candesartan cilexetil)

Alphabetical Index


Drug Information of ATACAND

Product NDC: 0186-0032
Proprietary Name: ATACAND
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 ATACAND

Product NDC: 0186-0032
Labeler Name: AstraZeneca LP
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020838
Marketing Category: NDA
Start Marketing Date: 19980914

Package Information of ATACAND

Package NDC: 0186-0032-54
Package Description: 90 TABLET in 1 BOTTLE (0186-0032-54)

NDC Information of ATACAND

NDC Code 0186-0032-54
Proprietary Name ATACAND
Package Description 90 TABLET in 1 BOTTLE (0186-0032-54)
Product NDC 0186-0032
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Candesartan cilexetil
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19980914
Marketing Category Name NDA
Labeler Name AstraZeneca LP
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 ATACAND


General Information