Triamterene and Hydrochlorothiazide is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Hydrochlorothiazide; Triamterene.
| Product ID | 71335-0968_5f5c3ada-db41-4104-9bed-9a56439a7ea2 |
| NDC | 71335-0968 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Triamterene and Hydrochlorothiazide |
| Generic Name | Triamterene And Hydrochlorothiazide |
| Dosage Form | Tablet |
| Route of Administration | ORAL |
| Marketing Start Date | 1993-09-23 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA073449 |
| Labeler Name | Bryant Ranch Prepack |
| Substance Name | HYDROCHLOROTHIAZIDE; TRIAMTERENE |
| Active Ingredient Strength | 25 mg/1; mg/1 |
| Pharm Classes | Decreased Renal K+ Excretion [PE], Increased Diuresis [PE], Increased Diuresis [PE], Potassium-sparing Diuretic [EPC], Thiazide Diuretic [EPC], Thiazides [CS] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2023-12-31 |
| Marketing Start Date | 2018-10-26 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA073449 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2013-01-24 |
| Marketing Category | ANDA |
| Application Number | ANDA073449 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2013-01-24 |
| Marketing Category | ANDA |
| Application Number | ANDA073449 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2013-01-24 |
| Ingredient | Strength |
|---|---|
| TRIAMTERENE | 37.5 mg/1 |
| SPL SET ID: | 5f5c3ada-db41-4104-9bed-9a56439a7ea2 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |