losartan potassium and hydrochlorothiazide
- Product NDC
- 29300-192
- 11-digit product format
- 293000192
- Labeler code
- 29300
- Product ID
- 29300-192_ad6e4664-08b6-4480-a1fb-6663c8024fef
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- losartan potassium and hydrochlorothiazide
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Unichem Pharmaceuticals (USA), Inc.
- Application
- ANDA204832
- Marketing category
- ANDA
- Marketing start
- 2017-07-21
- 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
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 | 25 mg/1 |
| LOSARTAN POTASSIUM | 100 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 3ST302B24A, 0J48LPH2TH |
| Rxcui | 979464, 979468, 979471 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 29300-192-01 | losartan potassium and hydrochlorothiazide | 100 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 100 | | 12 |
| 29300-192-10 | losartan potassium and hydrochlorothiazide | 1000 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 1000 | | 12 |
| 29300-192-13 | losartan potassium and hydrochlorothiazide | 30 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 30 | | 12 |
| 29300-192-19 | losartan potassium and hydrochlorothiazide | 90 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 90 | | 12 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 29300-192 | LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE TABLET, FILM COATED [UNICHEM PHARMACEUTICALS (USA), INC.] | 11 | Current NDC, Legacy NDC, 4 package rows | 20230418_f61b4ffe-cca6-482d-88fa-adf22cb3fff2.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 29300-192-01 | 29300019201 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-192-01) | 2018-01-15 | 0000-00-00 | No | No | Current |
| 29300-192-10 | 29300019210 | 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-192-10) | 2018-01-15 | 0000-00-00 | No | No | Current |
| 29300-192-13 | 29300019213 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-192-13) | 2018-01-15 | 0000-00-00 | No | No | Current |
| 29300-192-19 | 29300019219 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-192-19) | 2018-01-15 | 0000-00-00 | No | No | Current |