LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE
- Product NDC
- 72189-288
- 11-digit product format
- 721890288
- Labeler code
- 72189
- Product ID
- 72189-288_2c2941f2-b8cb-a99a-e063-6294a90ab626
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- DirectRx
- Application
- ANDA091629
- Marketing category
- ANDA
- Marketing start
- 2021-10-26
- Substance
- HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM
- Active strength
- 25; 100 mg/1; mg/1
- Pharmacologic classes
- Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 0J48LPH2TH | HYDROCHLOROTHIAZIDE | 58-93-5 | HYDROCHLOROTHIAZIDE |
| 3ST302B24A | LOSARTAN POTASSIUM | 124750-99-8 | LOSARTAN POTASSIUM |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 72189-288-90 | 72189028890 | 90 TABLET, FILM COATED in 1 BOTTLE (72189-288-90) | 2021-10-26 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Losartan Pot/HCTZ | DirectRx | 2025-01-20 | HUMAN PRESCRIPTION DRUG LABEL | 3 |