Losartan potassium
- Product NDC
- 61919-877
- 11-digit product format
- 619190877
- Labeler code
- 61919
- Product ID
- 61919-877_94e42fe5-77df-32c8-e053-2a95a90a643c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA090083
- Marketing category
- ANDA
- Marketing start
- 2019-06-03
- 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
- 2020-12-31
- 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 |
|---|
| 61919-877-30 | Losartan potassium | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 2 |
| 61919-877-90 | Losartan potassium | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61919-877 | LOSARTAN POTASSIUM TABLET, FILM COATED [DIRECT_RX] | 2 | Legacy NDC, 2 package rows | 20191015_8a70d474-ee10-67b1-e053-2a95a90ac946.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 |
|---|
| 61919-877-30 | 61919087730 | 30 TABLET, FILM COATED in 1 BOTTLE (61919-877-30) | 2019-06-03 | 0000-00-00 | No | No | Current |
| 61919-877-90 | 61919087790 | 90 TABLET, FILM COATED in 1 BOTTLE (61919-877-90) | 2019-06-03 | 0000-00-00 | No | No | Current |