Losartan Potassium and Hydrochlorothiazide
- Product NDC
- 71335-2560
- 11-digit product format
- 713352560
- Labeler code
- 71335
- Product ID
- 71335-2560_246381f3-31b9-4067-80f9-f3634e063b10
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- losartan potassium and hydrochlorothiazide
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA204901
- Marketing category
- ANDA
- Marketing start
- 2018-02-15
- Substance
- HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM
- Active strength
- 25; 100 mg/1; mg/1
- Pharmacologic classes
- Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC], Increased Diuresis [PE], 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 |
| 3ST302B24A | LOSARTAN POTASSIUM | 124750-99-8 | LOSARTAN POTASSIUM |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2560-1 | 71335256001 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-2560-1) | 2025-01-24 | No | No | Historical |
| 71335-2560-2 | 71335256002 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-2560-2) | 2025-01-24 | No | No | Historical |
| 71335-2560-3 | 71335256003 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-2560-3) | 2025-01-24 | No | No | Historical |