Losartan Potassium 68382-0135
Product NDC
68382-0135- Manufacturer
- Zydus Pharmaceuticals Usa Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- October 4, 2010
- Listing Expires
- December 31, 2027
- Application
- ANDA078243
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Losartan Potassium | 25 mg/1 |
Drug Class
Angiotensin 2 Receptor Antagonists [MoA]Angiotensin 2 Receptor Blocker [EPC]
Packaging Options(5)
100 TABLET, FILM COATED in 1 BOTTLE (68382-135-01)
30 TABLET, FILM COATED in 1 BOTTLE (68382-135-06)
1000 TABLET, FILM COATED in 1 BOTTLE (68382-135-10)
90 TABLET, FILM COATED in 1 BOTTLE (68382-135-16)
10000 TABLET, FILM COATED in 1 BOTTLE (68382-135-24)