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Candesartan Cilexetil and Hydrochlorothiazide
Candesartan Cilexetil and Hydrochlorothiazide - 60505-3760-9 - (Candesartan Cilexetil and Hydrochlorothiazide)
Drug Information of Candesartan Cilexetil and Hydrochlorothiazide
| Product NDC: | 60505-3760 |
| Proprietary Name: | Candesartan Cilexetil and Hydrochlorothiazide |
| Non Proprietary Name: | Candesartan Cilexetil and Hydrochlorothiazide |
| Active Ingredient(s): | 32; 25 mg/1; mg/1 & nbsp; Candesartan Cilexetil and Hydrochlorothiazide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Candesartan Cilexetil and Hydrochlorothiazide
| Product NDC: | 60505-3760 |
| Labeler Name: | Apotex Corp. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA202884 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130603 |
Package Information of Candesartan Cilexetil and Hydrochlorothiazide
| Package NDC: | 60505-3760-9 |
| Package Description: | 90 TABLET in 1 BOTTLE (60505-3760-9) |
NDC Information of Candesartan Cilexetil and Hydrochlorothiazide
| NDC Code | 60505-3760-9 |
| Proprietary Name | Candesartan Cilexetil and Hydrochlorothiazide |
| Package Description | 90 TABLET in 1 BOTTLE (60505-3760-9) |
| Product NDC | 60505-3760 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Candesartan Cilexetil and Hydrochlorothiazide |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20130603 |
| Marketing Category Name | ANDA |
| Labeler Name | Apotex Corp. |
| Substance Name | CANDESARTAN CILEXETIL; HYDROCHLOROTHIAZIDE |
| Strength Number | 32; 25 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] |
