NDC 70518-3420 – Losartan Potassium and Hydrochlorothiazide
Losartan Potassium 100 mg/1; Hydrochlorothiazide 25 mg/1 · Tablet, Film Coated · Oral
Product NDC70518-3420
Product details
- Brand name
- Losartan Potassium and Hydrochlorothiazide
- Generic name
- Losartan potassium and hydrochlorothiazide
- Labeler
- REMEDYREPACK INC.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA204901
- Marketed since
- May 16, 2022
- 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 (2)
| Package NDC | Description | Since |
|---|---|---|
| 70518-3420-2 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3420-2) | Aug 11, 2022 |
| 70518-3420-4 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3420-4) | Sep 13, 2025 |
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