Losartan Potassium
- Product NDC
- 43063-955
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan Potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA090083
- Marketing category
- ANDA
- Substance
- LOSARTAN POTASSIUM
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 43063-955-90 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-955-90) | 20190306 | | No | Historical |
Related DailyMed Labels
| Set ID | Title | Manufacturer | Effective date | Type | Version |
|---|
| 5f7612dc-dccf-49e2-b541-3dab9dc1f97a | These highlights do not include all the information needed to use LOSARTAN POTASSIUM TABLETS safely and effectively. See full prescribing information for LOSARTAN POTASSIUM TABLETS. LOSARTAN POTASSIUM tablets, for oral use Initial U.S. Approval: 1995 | PD-Rx Pharmaceuticals, Inc. | 2025-09-25 | HUMAN PRESCRIPTION DRUG LABEL | 28 |