NDC 31722-757 – Losartan Potassium And Hydrochlorothiazide
Losartan Potassium 100 mg/1; Hydrochlorothiazide 25 mg/1 · Tablet, Film Coated · Oral
Product NDC31722-757
Product details
- Brand name
- Losartan Potassium And Hydrochlorothiazide
- Generic name
- Losartan Potassium And Hydrochlorothiazide
- Labeler
- Camber Pharmaceuticals, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA219869
- Marketed since
- May 27, 2026
- Listing expires
- December 31, 2027
- 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 (3)
| Package NDC | Description | Since |
|---|---|---|
| 31722-757-10 | 1000 TABLET, FILM COATED in 1 BOTTLE (31722-757-10) | May 27, 2026 |
| 31722-757-30 | 30 TABLET, FILM COATED in 1 BOTTLE (31722-757-30) | May 27, 2026 |
| 31722-757-90 | 90 TABLET, FILM COATED in 1 BOTTLE (31722-757-90) | May 27, 2026 |
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