NDC 72789-162 – Losartan Potassium and Hydrochlorothiazide
Losartan Potassium 50 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet, Film Coated · Oral
Product NDC72789-162
Product details
- Brand name
- Losartan Potassium and Hydrochlorothiazide
- Generic name
- Losartan potassium and hydrochlorothiazide
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA201845
- Marketed since
- October 30, 2012
- 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 |
|---|---|---|
| 72789-162-30 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-162-30) | Jan 29, 2021 |
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