NDC 62332-050 – Losartan Potassium and Hydrochlorothiazide
Losartan Potassium 100 mg/1; Hydrochlorothiazide 25 mg/1 · Tablet, Film Coated · Oral
Product NDC62332-050
Product details
- Brand name
- Losartan Potassium and Hydrochlorothiazide
- Generic name
- Losartan Potassium and Hydrochlorothiazide
- Labeler
- Alembic Pharmaceuticals Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA091617
- Marketed since
- May 23, 2016
- 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 (4)
| Package NDC | Description | Since |
|---|---|---|
| 62332-050-10 | 100 BLISTER PACK in 1 CARTON (62332-050-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK | May 23, 2016 |
| 62332-050-30 | 30 TABLET, FILM COATED in 1 BOTTLE (62332-050-30) | May 23, 2016 |
| 62332-050-90 | 90 TABLET, FILM COATED in 1 BOTTLE (62332-050-90) | May 23, 2016 |
| 62332-050-91 | 1000 TABLET, FILM COATED in 1 BOTTLE (62332-050-91) | May 23, 2016 |
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