Home
>
National Drug Code (NDC)
>
edarbi
edarbi - 64764-884-07 - (Azilsartan kamedoxomil)
Drug Information of edarbi
| Product NDC: | 64764-884 |
| Proprietary Name: | edarbi |
| Non Proprietary Name: | Azilsartan kamedoxomil |
| Active Ingredient(s): | 80 mg/1 & nbsp; Azilsartan kamedoxomil |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of edarbi
| Product NDC: | 64764-884 |
| Labeler Name: | Takeda Pharmaceuticals America, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA200796 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20110225 |
Package Information of edarbi
| Package NDC: | 64764-884-07 |
| Package Description: | 5 CARTON in 1 TRAY (64764-884-07) > 1 BLISTER PACK in 1 CARTON > 7 TABLET in 1 BLISTER PACK |
NDC Information of edarbi
| NDC Code | 64764-884-07 |
| Proprietary Name | edarbi |
| Package Description | 5 CARTON in 1 TRAY (64764-884-07) > 1 BLISTER PACK in 1 CARTON > 7 TABLET in 1 BLISTER PACK |
| Product NDC | 64764-884 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Azilsartan kamedoxomil |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20110225 |
| Marketing Category Name | NDA |
| Labeler Name | Takeda Pharmaceuticals America, Inc. |
| Substance Name | AZILSARTAN KAMEDOXOMIL |
| Strength Number | 80 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Angiotensin 2 Type 1 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC],Decreased Blood Pressure [PE] |
