Losartan Potassium
- Product NDC
- 50090-2622
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan Potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA090083
- Marketing category
- ANDA
- Substance
- LOSARTAN POTASSIUM
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 50090-2622-0 | 30 TABLET, FILM COATED in 1 BOTTLE (50090-2622-0) | 2016-12-07 | | No | Historical |
| 50090-2622-1 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-2622-1) | 2016-11-16 | | No | Historical |
| 50090-2622-2 | 100 TABLET, FILM COATED in 1 BOTTLE (50090-2622-2) | 2023-10-26 | | No | Historical |