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Micardis HCT
Micardis HCT - 0597-0042-37 - (telmisartan and hydrochlorothiazide)
Drug Information of Micardis HCT
| Product NDC: | 0597-0042 |
| Proprietary Name: | Micardis HCT |
| Non Proprietary Name: | telmisartan and hydrochlorothiazide |
| Active Ingredient(s): | 25; 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: | 0597-0042 |
| Labeler Name: | Boehringer Ingelheim Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021162 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20001201 |
Package Information of Micardis HCT
| Package NDC: | 0597-0042-37 |
| Package Description: | 3 BLISTER PACK in 1 CARTON (0597-0042-37) > 10 TABLET in 1 BLISTER PACK |
NDC Information of Micardis HCT
| NDC Code | 0597-0042-37 |
| Proprietary Name | Micardis HCT |
| Package Description | 3 BLISTER PACK in 1 CARTON (0597-0042-37) > 10 TABLET in 1 BLISTER PACK |
| Product NDC | 0597-0042 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | telmisartan and hydrochlorothiazide |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20001201 |
| Marketing Category Name | NDA |
| Labeler Name | Boehringer Ingelheim Pharmaceuticals, Inc. |
| Substance Name | HYDROCHLOROTHIAZIDE; TELMISARTAN |
| Strength Number | 25; 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] |
