Losartan Potassium and Hydrochlorothiazide
- Product NDC
- 50090-4301
- 11-digit product format
- 500904301
- Labeler code
- 50090
- Product ID
- 50090-4301_b7f6a141-8671-43e7-af63-e904f6d04078
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan Potassium and Hydrochlorothiazide
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA091629
- Marketing category
- ANDA
- Marketing start
- 2010-10-06
- Marketing end
- 0000-00-00
- Substance
- LOSARTAN POTASSIUM; HYDROCHLOROTHIAZIDE
- Active strength
- 50 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 3ST302B24A | LOSARTAN POTASSIUM | 124750-99-8 | LOSARTAN POTASSIUM |
| 0J48LPH2TH | HYDROCHLOROTHIAZIDE | 58-93-5 | HYDROCHLOROTHIAZIDE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-4301-0 | 50090430100 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-4301-0) | 2019-05-20 | 0000-00-00 | No | No | Current |
| 50090-4301-1 | 50090430101 | 30 TABLET, FILM COATED in 1 BOTTLE (50090-4301-1) | 2019-05-16 | 0000-00-00 | No | No | Current |