Edarbyclor - 64764-994-07 - (azilsartan medoxomil and chlorthalidone)

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Drug Information of Edarbyclor

Product NDC: 64764-994
Proprietary Name: Edarbyclor
Non Proprietary Name: azilsartan medoxomil and chlorthalidone
Active Ingredient(s): 40; 25    mg/1; mg/1 & nbsp;   azilsartan medoxomil and chlorthalidone
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Edarbyclor

Product NDC: 64764-994
Labeler Name: Takeda Pharmaceuticals America, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA202331
Marketing Category: NDA
Start Marketing Date: 20111223

Package Information of Edarbyclor

Package NDC: 64764-994-07
Package Description: 5 CARTON in 1 TRAY (64764-994-07) > 1 BLISTER PACK in 1 CARTON > 7 TABLET in 1 BLISTER PACK

NDC Information of Edarbyclor

NDC Code 64764-994-07
Proprietary Name Edarbyclor
Package Description 5 CARTON in 1 TRAY (64764-994-07) > 1 BLISTER PACK in 1 CARTON > 7 TABLET in 1 BLISTER PACK
Product NDC 64764-994
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name azilsartan medoxomil and chlorthalidone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20111223
Marketing Category Name NDA
Labeler Name Takeda Pharmaceuticals America, Inc.
Substance Name AZILSARTAN KAMEDOXOMIL; CHLORTHALIDONE
Strength Number 40; 25
Strength Unit mg/1; mg/1
Pharmaceutical Classes Angiotensin 2 Type 1 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC],Decreased Blood Pressure [PE],Increased Diuresis [PE],Thiazide-like Diuretic [EPC]

Complete Information of Edarbyclor


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