Losartan Potassium
- Product NDC
- 53002-3643
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan Potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- RPK Pharmaceuticals, Inc.
- 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 |
|---|
| 53002-3643-0 | 100 TABLET, FILM COATED in 1 BOTTLE (53002-3643-0) | 2019-01-01 | 0000-00-00 | No | Current |
| 53002-3643-3 | 30 TABLET, FILM COATED in 1 BOTTLE (53002-3643-3) | 2019-01-01 | 0000-00-00 | No | Current |
| 53002-3643-9 | 90 TABLET, FILM COATED in 1 BOTTLE (53002-3643-9) | 2019-01-01 | 0000-00-00 | No | Current |