NDC 68071-4159 – Losartan Potassium and Hydrochlorothiazide
Losartan Potassium 100 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet, Film Coated · Oral
Product NDC68071-4159
Product details
- Brand name
- Losartan Potassium and Hydrochlorothiazide
- Generic name
- Losartan Potassium and Hydrochlorothiazide
- Labeler
- NuCare Pharmaceuticals,Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA091617
- Marketed since
- May 23, 2016
- Listing expires
- December 31, 2026
- Pharmacologic class
- Angiotensin 2 Receptor Blocker; Thiazide Diuretic
Active ingredients
- Losartan Potassium 100 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 |
|---|---|---|
| 68071-4159-3 | 30 TABLET, FILM COATED in 1 BOTTLE (68071-4159-3) | Nov 17, 2017 |
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