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Micardis HCT
Micardis HCT - 35356-299-30 - (TELMISARTAN AND HYDROCHLOROTHIAZIDE)
Drug Information of Micardis HCT
| Product NDC: | 35356-299 |
| Proprietary Name: | Micardis HCT |
| Non Proprietary Name: | TELMISARTAN AND HYDROCHLOROTHIAZIDE |
| Active Ingredient(s): | 12.5; 80 mg/1; mg/1 & nbsp; TELMISARTAN AND HYDROCHLOROTHIAZIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Micardis HCT
| Product NDC: | 35356-299 |
| Labeler Name: | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021162 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20120315 |
Package Information of Micardis HCT
| Package NDC: | 35356-299-30 |
| Package Description: | 3 BLISTER PACK in 1 CARTON (35356-299-30) > 10 TABLET in 1 BLISTER PACK |
NDC Information of Micardis HCT
| NDC Code | 35356-299-30 |
| Proprietary Name | Micardis HCT |
| Package Description | 3 BLISTER PACK in 1 CARTON (35356-299-30) > 10 TABLET in 1 BLISTER PACK |
| Product NDC | 35356-299 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | TELMISARTAN AND HYDROCHLOROTHIAZIDE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20120315 |
| Marketing Category Name | NDA |
| Labeler Name | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC |
| Substance Name | HYDROCHLOROTHIAZIDE; TELMISARTAN |
| Strength Number | 12.5; 80 |
| 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] |
