NDC 82804-239 – Losartan Potassium and Hydrochlorothiazide
Losartan Potassium 50 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet, Film Coated · Oral
Product NDC82804-239
Product details
- Brand name
- Losartan Potassium and Hydrochlorothiazide
- Generic name
- Losartan potassium and hydrochlorothiazide
- Labeler
- Proficient Rx LP
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA204901
- Marketed since
- February 15, 2018
- Listing expires
- December 31, 2026
- 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 (1)
| Package NDC | Description | Since |
|---|---|---|
| 82804-239-30 | 30 TABLET, FILM COATED in 1 BOTTLE (82804-239-30) | Sep 3, 2025 |
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