Losartan potassium Tablets, 25 mg
- Product NDC
- 72162-1696
- 11-digit product format
- 721621696
- Labeler code
- 72162
- Product ID
- 72162-1696_448a3184-c51b-450f-880c-4eb15084abf7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- losartan potassium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA201170
- Marketing category
- ANDA
- Marketing start
- 2012-09-18
- Substance
- LOSARTAN POTASSIUM
- Active strength
- 25 mg/1
- Pharmacologic classes
- Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC]
- 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 Tablets, 25 mg
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| LOSARTAN POTASSIUM | 25 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 3ST302B24A |
| Rxcui | 979485 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72162-1696-0 | Losartan potassium Tablets, 25 mg | 1000 in 1 BOTTLE | TABLET | 1000 | | 101 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72162-1696 | LOSARTAN POTASSIUM TABLETS, 25 MG (LOSARTAN POTASSIUM) TABLET [BRYANT RANCH PREPACK] | 100 | Current NDC, 1 package rows | 20240207_7b8f5329-4fdb-4e1d-98b1-de1ca1b171c5.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-1696-0 | 72162169600 | 1000 TABLET in 1 BOTTLE (72162-1696-0) | 1000 tablet | 2024-02-06 | No | No | Historical |