NDC 50090-1745 – Losartan Potassium and Hydrochlorothiazide
Losartan Potassium 100 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet, Film Coated · Oral
Product NDC50090-1745
Product details
- Brand name
- Losartan Potassium and Hydrochlorothiazide
- Generic name
- Losartan Potassium and Hydrochlorothiazide
- Labeler
- A-S Medication Solutions
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA091629
- Marketed since
- October 6, 2010
- Listing expires
- December 31, 2027
- Pharmacologic class
- Angiotensin 2 Receptor Blocker; Thiazide Diuretic
Active ingredients
- Losartan Potassium 100 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 |
|---|---|---|
| 50090-1745-0 | 30 TABLET, FILM COATED in 1 BOTTLE (50090-1745-0) | Mar 17, 2015 |
| 50090-1745-1 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-1745-1) | Mar 17, 2015 |
| 50090-1745-2 | 100 TABLET, FILM COATED in 1 BOTTLE (50090-1745-2) | Sep 26, 2024 |
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