Losartan Potassium 68788-7665
Product NDC
68788-7665- Manufacturer
- Preferred Pharmaceuticals, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- February 28, 2020
- Listing Expires
- December 31, 2027
- Application
- ANDA203835
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Losartan Potassium | 50 mg/1 |
Drug Class
Angiotensin 2 Receptor Antagonists [MoA]Angiotensin 2 Receptor Blocker [EPC]
Packaging Options(4)
100 TABLET, FILM COATED in 1 BOTTLE (68788-7665-1)
30 TABLET, FILM COATED in 1 BOTTLE (68788-7665-3)
60 TABLET, FILM COATED in 1 BOTTLE (68788-7665-6)
90 TABLET, FILM COATED in 1 BOTTLE (68788-7665-9)