Losartan Potassium And Hydrochlorothiazide 65862-0470
Product NDC
65862-0470- Manufacturer
- Aurobindo Pharma Limited
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- October 6, 2010
- Listing Expires
- December 31, 2026
- Application
- ANDA091629
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Hydrochlorothiazide | 25 mg/1 |
| Losartan Potassium | 100 mg/1 |
Drug Class
Thiazide Diuretic [EPC]Angiotensin 2 Receptor Antagonists [MoA]Angiotensin 2 Receptor Blocker [EPC]
Packaging Options(5)
10 BLISTER PACK in 1 CARTON (65862-470-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK
30 TABLET, FILM COATED in 1 BOTTLE (65862-470-30)
5000 TABLET, FILM COATED in 1 BOTTLE (65862-470-59)
90 TABLET, FILM COATED in 1 BOTTLE (65862-470-90)
1000 TABLET, FILM COATED in 1 BOTTLE (65862-470-99)