NDC 72189-297 – Losartan Potassium And Hydrochlorothiazide
Hydrochlorothiazide 12.5 mg/1; Losartan Potassium 50 mg/1 · Tablet, Film Coated · Oral
Product NDC72189-297
Product details
- Brand name
- Losartan Potassium And Hydrochlorothiazide
- Generic name
- Losartan Potassium And Hydrochlorothiazide
- Labeler
- DirectRx
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA202289
- Marketed since
- November 30, 2021
- 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 (1)
| Package NDC | Description | Since |
|---|---|---|
| 72189-297-90 | 90 TABLET, FILM COATED in 1 BOTTLE (72189-297-90) | Nov 30, 2021 |
Recalls mentioning this NDC
- D-0894-2022 Jun 1, 2022 · Class II
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits .
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