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