Losartan Potassium
- Product NDC
- 68788-8189
- 11-digit product format
- 687888189
- Labeler code
- 68788
- Product ID
- 68788-8189_061d0838-f325-4fdb-8eb5-c0684f0df7db
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA091497
- Marketing category
- ANDA
- Marketing start
- 2022-05-13
- Substance
- LOSARTAN POTASSIUM
- Active strength
- 50 mg/1
- Pharmacologic classes
- Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 3ST302B24A | LOSARTAN POTASSIUM | 124750-99-8 | LOSARTAN POTASSIUM |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 68788-8189-1 | 68788818901 | 100 TABLET, FILM COATED in 1 BOTTLE (68788-8189-1) | 2022-05-13 | No | No | Historical |
| 68788-8189-3 | 68788818903 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-8189-3) | 2022-05-13 | No | No | Historical |
| 68788-8189-6 | 68788818906 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-8189-6) | 2022-05-13 | No | No | Historical |
| 68788-8189-9 | 68788818909 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-8189-9) | 2022-05-13 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Losartan Potassium | Preferred Pharmaceuticals Inc. | 2025-08-01 | HUMAN PRESCRIPTION DRUG LABEL | 4 |