Losartan potassium
- Product NDC
- 61919-877
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA090083
- Marketing category
- ANDA
- Substance
- LOSARTAN POTASSIUM
- Current FDA listing
- Historical FDA.report record
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 61919-877-30 | 30 TABLET, FILM COATED in 1 BOTTLE (61919-877-30) | 2019-06-03 | 0000-00-00 | No | Current |
| 61919-877-90 | 90 TABLET, FILM COATED in 1 BOTTLE (61919-877-90) | 2019-06-03 | 0000-00-00 | No | Current |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| LOSARTAN POTASSIUM | Direct_Rx | 2019-10-14 | HUMAN PRESCRIPTION DRUG LABEL | 2 |