Triamterene and Hydrochlorothiazide is a Oral Capsule in the Human Prescription Drug category. It is labeled and distributed by Mylan Pharmaceuticals Inc.. The primary component is Hydrochlorothiazide; Triamterene.
| Product ID | 0378-2537_0d1633a2-b296-46ac-aef2-70a05e86611e |
| NDC | 0378-2537 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Triamterene and Hydrochlorothiazide |
| Generic Name | Triamterene And Hydrochlorothiazide |
| Dosage Form | Capsule |
| Route of Administration | ORAL |
| Marketing Start Date | 1996-06-07 |
| Marketing End Date | 2022-05-31 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA074701 |
| Labeler Name | Mylan Pharmaceuticals Inc. |
| Substance Name | HYDROCHLOROTHIAZIDE; TRIAMTERENE |
| Active Ingredient Strength | 25 mg/1; mg/1 |
| Pharm Classes | Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS],Decreased Renal K+ Excretion [PE],Increased Diuresis [PE],Potassium-sparing Diuretic [EPC] |
| NDC Exclude Flag | N |
| Marketing Start Date | 1996-06-07 |
| Marketing End Date | 2022-05-31 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA074701 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1996-06-07 |
| Marketing Category | ANDA |
| Application Number | ANDA074701 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1996-06-07 |
| Ingredient | Strength |
|---|---|
| HYDROCHLOROTHIAZIDE | 25 mg/1 |
| SPL SET ID: | 1c1277f3-1936-40f2-8efa-4233c39f93a0 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |