LOSARTAN POTASSIUM
- Product NDC
- 61919-952
- 11-digit product format
- 619190952
- Labeler code
- 61919
- Product ID
- 61919-952_9c98c7c9-b1a2-292f-e053-2a95a90a69fb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- LOSARTAN POTASSIUM
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA090467
- Marketing category
- ANDA
- Marketing start
- 2019-08-21
- Marketing end
- 0000-00-00
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 61919-952-90 | LOSARTAN POTASSIUM | 90 in 1 BOTTLE | TABLET | 90 | | 6 |
| 61919-952-30 | LOSARTAN POTASSIUM | 30 in 1 BOTTLE | TABLET | 30 | | 2 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61919-952 | LOSARTAN POTASSIUM TABLET [DIRECT RX] | 6 | Legacy NDC, 1 package rows | 20161115_d6ba182e-b768-4913-8688-7f29676b05c9.zip |
| 61919-952 | LOSARTAN POTASSIUM TABLET [DIRECT_RX] | 2 | Legacy NDC, 1 package rows | 20200121_90a2b710-574a-4f49-e053-2995a90ad2a9.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 |
|---|
| 61919-952-30 | 61919095230 | 30 TABLET in 1 BOTTLE (61919-952-30) | 30 tablet | 2019-08-21 | 0000-00-00 | No | No | Current |
| 61919-952-90 | 61919095290 | 90 in 1 BOTTLE | | | | | | Historical |