NDC 43547-423 – Losartan Potassium and Hydrochlorothiazide
Losartan Potassium 50 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet, Film Coated · Oral
Product NDC43547-423
Product details
- Brand name
- Losartan Potassium and Hydrochlorothiazide
- Generic name
- Losartan potassium and hydrochlorothiazide
- Labeler
- Solco Healthcare US, LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA204901
- Marketed since
- February 15, 2018
- Listing expires
- December 31, 2027
- Pharmacologic class
- Angiotensin 2 Receptor Blocker; Thiazide Diuretic
Active ingredients
- Losartan Potassium 50 mg/1
- Hydrochlorothiazide 12.5 mg/1
Uses, dosage, side effects and warnings for Losartan Potassium and Hydrochlorothiazide →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 43547-423-03 | 30 TABLET, FILM COATED in 1 BOTTLE (43547-423-03) | Feb 15, 2018 |
| 43547-423-09 | 90 TABLET, FILM COATED in 1 BOTTLE (43547-423-09) | Feb 15, 2018 |
| 43547-423-11 | 1000 TABLET, FILM COATED in 1 BOTTLE (43547-423-11) | Feb 15, 2018 |
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