Losartan potassium
- Product NDC
- 72205-141
- 11-digit product format
- 722050141
- Labeler code
- 72205
- Product ID
- 72205-141_965852b8-5563-4f23-8cd1-a2f82cf16d3f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Novadoz Pharmaceuticals LLC
- Application
- ANDA217396
- Marketing category
- ANDA
- Marketing start
- 2023-08-14
- 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
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Losartan potassium
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| LOSARTAN POTASSIUM | 25 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 3ST302B24A |
| Rxcui | 979480, 979485, 979492 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72205-141-90 | Losartan potassium | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | | 3 |
| 72205-141-99 | Losartan potassium | 1000 in 1 BOTTLE | TABLET, FILM COATED | 1000 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72205-141 | LOSARTAN POTASSIUM TABLET, FILM COATED [NOVADOZ PHARMACEUTICALS LLC] | 1 | Current NDC, 2 package rows | 20230819_5edb843a-66ed-4950-9ed0-393e6a5d7c99.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 72205-141-90 | 72205014190 | 90 TABLET, FILM COATED in 1 BOTTLE (72205-141-90) | 2023-08-16 | No | No | Current |
| 72205-141-99 | 72205014199 | 1000 TABLET, FILM COATED in 1 BOTTLE (72205-141-99) | 2023-08-16 | No | No | Current |