NDC 68071-4518 – Losartan Potassium and Hydrochlorothiazide
Losartan Potassium 100 mg/1; Hydrochlorothiazide 25 mg/1 · Tablet, Film Coated · Oral
Product NDC68071-4518
Product details
- Brand name
- Losartan Potassium and Hydrochlorothiazide
- Generic name
- Losartan Potassium and Hydrochlorothiazide
- Labeler
- NuCare Pharmaceuticals,Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA077157
- Marketed since
- April 6, 2010
- Listing expires
- December 31, 2026
- Pharmacologic class
- Angiotensin 2 Receptor Blocker; Thiazide Diuretic
Active ingredients
- Losartan Potassium 100 mg/1
- Hydrochlorothiazide 25 mg/1
Uses, dosage, side effects and warnings for Losartan Potassium and Hydrochlorothiazide →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 68071-4518-3 | 30 TABLET, FILM COATED in 1 BOTTLE (68071-4518-3) | Aug 6, 2018 |
| 68071-4518-9 | 90 TABLET, FILM COATED in 1 BOTTLE (68071-4518-9) | Aug 6, 2018 |
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