NDC 72189-129 – Losartan Potassium And Hydrochlorothiazide
Hydrochlorothiazide 12.5 mg/1; Losartan Potassium 50 mg/1 · Tablet, Film Coated · Oral
Product NDC72189-129
Product details
- Brand name
- Losartan Potassium And Hydrochlorothiazide
- Generic name
- Losartan potassium and hydrochlorothiazide
- Labeler
- Direct_Rx
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA201845
- Marketed since
- October 15, 2020
- Listing expires
- December 31, 2026
- Pharmacologic class
- Angiotensin 2 Receptor Blocker; Thiazide Diuretic
Active ingredients
- Hydrochlorothiazide 12.5 mg/1
- Losartan Potassium 50 mg/1
Uses, dosage, side effects and warnings for Losartan Potassium and Hydrochlorothiazide →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 72189-129-30 | 30 TABLET, FILM COATED in 1 BOTTLE (72189-129-30) | Oct 15, 2020 |
| 72189-129-90 | 90 TABLET, FILM COATED in 1 BOTTLE (72189-129-90) | Oct 15, 2020 |
Recalls mentioning this NDC
- D-0971-2022 Jun 8, 2022 · Class II
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
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