Losartan potassium Tablets, 50 mg
- Product NDC
- 63629-9192
- 11-digit product format
- 636299192
- Labeler code
- 63629
- Product ID
- 63629-9192_13337021-409e-4c0c-b7ee-3c40b442828d
- 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
- 50 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, 50 mg
- Listing expiration
- 2026-12-31
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 |
|---|
| 63629-9192-1 | Losartan potassium Tablets, 50 mg | 1000 in 1 BOTTLE | TABLET | 1000 | | 103 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63629-9192 | LOSARTAN POTASSIUM TABLETS, 50 MG (LOSARTAN POTASSIUM) TABLET [BRYANT RANCH PREPACK] | 102 | Current NDC, Legacy NDC, 1 package rows | 20240113_eea03814-3fb5-4f85-8a4d-18e73057d880.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-9192-1 | 63629919201 | 1000 TABLET in 1 BOTTLE (63629-9192-1) | 1000 tablet | 2022-08-03 | 0000-00-00 | No | No | Current |