NDC 68788-8187 – Losartan Potassium and Hydrochlorothiazide
Losartan Potassium 50 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet, Film Coated · Oral
Product NDC68788-8187
Product details
- Brand name
- Losartan Potassium and Hydrochlorothiazide
- Generic name
- Losartan potassium and hydrochlorothiazide
- Labeler
- Preferred Pharmaceuticals Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA204901
- Marketed since
- May 10, 2022
- 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 (4)
| Package NDC | Description | Since |
|---|---|---|
| 68788-8187-1 | 100 TABLET, FILM COATED in 1 BOTTLE (68788-8187-1) | May 10, 2022 |
| 68788-8187-3 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-8187-3) | May 10, 2022 |
| 68788-8187-6 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-8187-6) | May 10, 2022 |
| 68788-8187-9 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-8187-9) | May 10, 2022 |
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