Losartan Potassium
- Product NDC
- 68071-5175
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan Potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA203835
- Marketing category
- ANDA
- Substance
- LOSARTAN POTASSIUM
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 68071-5175-9 | 90 TABLET, FILM COATED in 1 BOTTLE (68071-5175-9) | 2020-08-26 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Losartan Potassium | NuCare Pharmaceuticals,Inc. | 2025-02-04 | HUMAN PRESCRIPTION DRUG LABEL | 3 |