Losartan Potassium
- Product NDC
- 72189-303
- 11-digit product format
- 721890303
- Labeler code
- 72189
- Product ID
- 72189-303_2c295943-f8ca-fd38-e063-6394a90ad5cf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan Potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- DirectRx
- Application
- ANDA203835
- Marketing category
- ANDA
- Marketing start
- 2021-12-17
- 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
- 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 |
|---|
| 72189-303-90 | Losartan Potassium | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72189-303 | LOSARTAN POTASSIUM TABLET, FILM COATED [DIRECTRX] | 2 | Current NDC, Legacy NDC, 1 package rows | 20250121_d358499d-5ebb-75b2-e053-2a95a90a4223.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 |
|---|
| 72189-303-90 | 72189030390 | 90 TABLET, FILM COATED in 1 BOTTLE (72189-303-90) | 2021-12-17 | 0000-00-00 | No | No | Current |