NDC 0904-7034
Candesartan
Candesartan
Candesartan is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Major Pharmaceuticals. The primary component is Candesartan Cilexetil.
| Product ID | 0904-7034_07ac7ec0-c9ef-4d3d-a6c6-9b042e93699c |
| NDC | 0904-7034 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Candesartan |
| Generic Name | Candesartan |
| Dosage Form | Tablet |
| Route of Administration | ORAL |
| Marketing Start Date | 2016-12-06 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA203813 |
| Labeler Name | Major Pharmaceuticals |
| Substance Name | CANDESARTAN CILEXETIL |
| Active Ingredient Strength | 32 mg/1 |
| Pharm Classes | Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2022-12-31 |