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Azor
Azor - 65597-111-07 - (amlodipine besylate and olmesartan medoxomil)
Drug Information of Azor
| Product NDC: | 65597-111 |
| Proprietary Name: | Azor |
| Non Proprietary Name: | amlodipine besylate and olmesartan medoxomil |
| Active Ingredient(s): | 10; 20 mg/1; mg/1 & nbsp; amlodipine besylate and olmesartan medoxomil |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Azor
| Product NDC: | 65597-111 |
| Labeler Name: | Daiichi Sankyo, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022100 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20070926 |
Package Information of Azor
| Package NDC: | 65597-111-07 |
| Package Description: | 7 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (65597-111-07) |
NDC Information of Azor
| NDC Code | 65597-111-07 |
| Proprietary Name | Azor |
| Package Description | 7 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (65597-111-07) |
| Product NDC | 65597-111 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | amlodipine besylate and olmesartan medoxomil |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20070926 |
| Marketing Category Name | NDA |
| Labeler Name | Daiichi Sankyo, Inc. |
| Substance Name | AMLODIPINE BESYLATE; OLMESARTAN MEDOXOMIL |
| Strength Number | 10; 20 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient],Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC] |
