NDC 16714-226 – Losartan Potassium and Hydrochlorothiazide
Losartan Potassium 50 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet, Film Coated · Oral
Product NDC16714-226
Product details
- Brand name
- Losartan Potassium and Hydrochlorothiazide
- Generic name
- Losartan Potassium and Hydrochlorothiazide
- Labeler
- NorthStar Rx LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA091629
- Marketed since
- September 4, 2024
- 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 (3)
| Package NDC | Description | Since |
|---|---|---|
| 16714-226-01 | 30 TABLET, FILM COATED in 1 BOTTLE (16714-226-01) | Sep 4, 2024 |
| 16714-226-02 | 90 TABLET, FILM COATED in 1 BOTTLE (16714-226-02) | Sep 4, 2024 |
| 16714-226-04 | 1000 TABLET, FILM COATED in 1 BOTTLE (16714-226-04) | Sep 4, 2024 |
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