Losartan Potassium
- Product NDC
- 51655-828
- 11-digit product format
- 516550828
- Labeler code
- 51655
- Product ID
- 51655-828_4bbb871a-cd69-9870-e063-6394a90a0189
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan Potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Northwind Health Company, LLC
- Application
- ANDA203835
- Marketing category
- ANDA
- Marketing start
- 2022-02-21
- Substance
- LOSARTAN POTASSIUM
- Active strength
- 100 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 | 100 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 3ST302B24A |
| Rxcui | 979480 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51655-828-26 | Losartan Potassium | 90 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 90 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51655-828 | LOSARTAN POTASSIUM TABLET, FILM COATED [NORTHWIND PHARMACEUTICALS] | 2 | Current NDC, Legacy NDC, 1 package rows | 20231219_d9df33c8-4ea7-5d1c-e053-2a95a90aecf7.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 |
|---|
| 51655-828-26 | 51655082826 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-828-26) | 2022-02-21 | 0000-00-00 | No | No | Current |