Olmesartan Medoxomil and Hydrochlorothiazide
- Product NDC
- 50090-5909
- 11-digit product format
- 500905909
- Labeler code
- 50090
- Product ID
- 50090-5909_397fa01f-c5e6-4fca-ac48-71e2a896eab3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Olmesartan Medoxomil and Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA204233
- Marketing category
- ANDA
- Marketing start
- 2017-04-24
- Marketing end
- 0000-00-00
- Substance
- HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL
- Active strength
- 13 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 0J48LPH2TH | HYDROCHLOROTHIAZIDE | 58-93-5 | HYDROCHLOROTHIAZIDE |
| 6M97XTV3HD | OLMESARTAN MEDOXOMIL | 144689-63-4 | OLMESARTAN MEDOXOMIL |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-5909-0 | 50090590900 | 30 TABLET in 1 BOTTLE (50090-5909-0) | 30 tablet | 2022-01-21 | 0000-00-00 | No | No | Current |
| 50090-5909-1 | 50090590901 | 90 TABLET in 1 BOTTLE (50090-5909-1) | 90 tablet | 2022-01-21 | 0000-00-00 | No | No | Current |