Triamterene and Hydrochlorothiazide
- Product NDC
- 50090-6944
- 11-digit product format
- 500906944
- Labeler code
- 50090
- Product ID
- 50090-6944_0eafe08c-9082-452e-b9d7-534647514f11
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Triamterene and Hydrochlorothiazide
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA074821
- Marketing category
- ANDA
- Marketing start
- 1997-06-05
- Substance
- HYDROCHLOROTHIAZIDE; TRIAMTERENE
- Active strength
- 25; 37.5 mg/1; mg/1
- Pharmacologic classes
- Decreased Renal K+ Excretion [PE], Increased Diuresis [PE], Increased Diuresis [PE], Potassium-sparing Diuretic [EPC], Thiazide Diuretic [EPC], Thiazides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 0J48LPH2TH | HYDROCHLOROTHIAZIDE | 58-93-5 | HYDROCHLOROTHIAZIDE |
| WS821Z52LQ | TRIAMTERENE | 396-01-0 | TRIAMTERENE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-6944-0 | 50090694400 | 90 CAPSULE in 1 BOTTLE (50090-6944-0) | 90 capsule | 2023-12-18 | No | No | Historical |