LOSARTAN POTASSIUM
- Product NDC
- 61919-461
- 11-digit product format
- 619190461
- Labeler code
- 61919
- Product ID
- 61919-461_9c98cd98-360a-2afa-e053-2a95a90af374
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- LOSARTAN POTASSIUM
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Direct Rx
- Application
- ANDA090467
- Marketing category
- ANDA
- Marketing start
- 2018-11-12
- Marketing end
- 0000-00-00
- 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
- 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 |
|---|
| 61919-461-30 | LOSARTAN POTASSIUM | 30 in 1 BOTTLE | TABLET | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61919-461 | LOSARTAN POTASSIUM TABLET [DIRECTRX] | 1 | Legacy NDC, 1 package rows | 20151203_25fe6b18-e408-4b17-e054-00144ff8d46c.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 |
|---|
| 61919-461-30 | 61919046130 | 30 in 1 BOTTLE | | | | | | Historical |
| 61919-461-90 | 61919046190 | 90 TABLET in 1 BOTTLE (61919-461-90) | 90 tablet | 2018-11-12 | 0000-00-00 | No | No | Current |