Dyrenium is a Oral Capsule in the Human Prescription Drug category. It is labeled and distributed by Concordia Pharmaceuticals Inc.. The primary component is Triamterene.
| Product ID | 59212-003_0818de3a-75e9-4c96-8cee-afeea533ef7c |
| NDC | 59212-003 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Dyrenium |
| Generic Name | Triamterene |
| Dosage Form | Capsule |
| Route of Administration | ORAL |
| Marketing Start Date | 1999-01-01 |
| Marketing Category | NDA / NDA |
| Application Number | NDA013174 |
| Labeler Name | Concordia Pharmaceuticals Inc. |
| Substance Name | TRIAMTERENE |
| Active Ingredient Strength | 100 mg/1 |
| Pharm Classes | Decreased Renal K+ Excretion [PE],Increased Diuresis [PE],Potassium-sparing Diuretic [EPC] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2021-12-31 |
| Marketing Start Date | 1999-01-01 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | NDA |
| Application Number | NDA013174 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1999-01-01 |
| Ingredient | Strength |
|---|---|
| TRIAMTERENE | 100 mg/1 |
| SPL SET ID: | ebb177c0-d45d-4443-a85a-e76bd9931a42 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | |
| UPC Code |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 59212-002 | Dyrenium | Triamterene |
| 59212-003 | Dyrenium | Triamterene |
| 65197-002 | Dyrenium | Triamterene |
| 65197-003 | Dyrenium | Triamterene |
| 68151-1494 | Dyrenium | Triamterene |
| 66993-831 | triamterene | Triamterene |
| 66993-832 | Triamterene | Triamterene |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() DYRENIUM 72193818 0785081 Live/Registered |
SMITH KLINE & FRENCH LABORATORIES 1964-05-19 |