Triamterene and Hydrochlorothiazide
- Product NDC
- 50090-1834
- 11-digit product format
- 500901834
- Labeler code
- 50090
- Product ID
- 50090-1834_b7aace6d-e542-4a86-9e45-8c2e690daca4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Triamterene and Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA071851
- Marketing category
- ANDA
- Marketing start
- 1993-09-23
- Substance
- HYDROCHLOROTHIAZIDE; TRIAMTERENE
- Active strength
- 50; 75 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 |
|---|
| 50090-1834-0 | 50090183400 | 30 TABLET in 1 BOTTLE (50090-1834-0) | 30 tablet | 2015-05-19 | No | No | Historical |
| 50090-1834-2 | 50090183402 | 100 TABLET in 1 BOTTLE (50090-1834-2) | 100 tablet | 2015-05-19 | No | No | Historical |
| 50090-1834-5 | 50090183405 | 90 TABLET in 1 BOTTLE (50090-1834-5) | 90 tablet | 2015-07-29 | No | No | Historical |