LOSARTAN POTASSIUM
- Product NDC
- 72789-179
- 11-digit product format
- 727890179
- Labeler code
- 72789
- Product ID
- 72789-179_4af906c5-4409-7659-e063-6394a90a49ee
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- LOSARTAN POTASSIUM
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA090382
- Marketing category
- ANDA
- Marketing start
- 2019-10-09
- Substance
- LOSARTAN POTASSIUM
- Active strength
- 50 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
- Brand name suffix
- 50 mg
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| LOSARTAN POTASSIUM | 50 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 3ST302B24A |
| Rxcui | 979492 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72789-179-90 | LOSARTAN POTASSIUM50 mg | 90 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 90 | | 9 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72789-179 | LOSARTAN POTASSIUM 50 MG (LOSARTAN POTASSIUM) TABLET, FILM COATED [PD-RX PHARMACEUTICALS, INC.] | 7 | Current NDC, Legacy NDC, 1 package rows | 20240719_498f26a1-5030-4f9b-9599-07d50e912d41.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 |
|---|
| 72789-179-90 | 72789017990 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-179-90) | 2021-03-24 | 0000-00-00 | No | No | Current |