losartan potassium and hydrochlorothiazide
- Product NDC
- 71335-2662
- 11-digit product format
- 713352662
- Labeler code
- 71335
- Product ID
- 71335-2662_de121cef-3137-4100-9489-f7c6a50faba8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- losartan potassium and hydrochlorothiazide
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA204832
- Marketing category
- ANDA
- Marketing start
- 2017-07-21
- Substance
- HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM
- Active strength
- 12.5; 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- losartan potassium and hydrochlorothiazide
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| HYDROCHLOROTHIAZIDE | 12.5 mg/1 |
| LOSARTAN POTASSIUM | 100 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 0J48LPH2TH, 3ST302B24A |
| Rxcui | 979464 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71335-2662-1 | losartan potassium and hydrochlorothiazide | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 100 |
| 71335-2662-2 | losartan potassium and hydrochlorothiazide | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | | 100 |
| 71335-2662-3 | losartan potassium and hydrochlorothiazide | 120 in 1 BOTTLE | TABLET, FILM COATED | 120 | | 100 |
| 71335-2662-4 | losartan potassium and hydrochlorothiazide | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | | 100 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2662-1 | 71335266201 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-2662-1) | 2025-06-26 | No | No | Current |
| 71335-2662-2 | 71335266202 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-2662-2) | 2025-06-26 | No | No | Current |
| 71335-2662-3 | 71335266203 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-2662-3) | 2025-06-26 | No | No | Current |
| 71335-2662-4 | 71335266204 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-2662-4) | 2025-06-26 | No | No | Current |