Olmesartan Medoxomil and Hydrochlorothiazide
- Product NDC
- 50090-6027
- 11-digit product format
- 500906027
- Labeler code
- 50090
- Product ID
- 50090-6027_70465daf-5475-4df5-a2cb-9c660851dd9a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Olmesartan Medoxomil and Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA208847
- Marketing category
- ANDA
- Marketing start
- 2020-10-01
- 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
DailyMed Product Concepts#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-6027 | OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE (OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE) TABLET [A-S MEDICATION SOLUTIONS] | 4 | Legacy NDC | 20231020_cb04f0b5-41af-4f66-ae9c-9dbfbd2db77c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-6027-0 | 50090602700 | 30 TABLET in 1 BOTTLE (50090-6027-0) | 30 tablet | 2022-06-30 | 0000-00-00 | No | No | Current |
| 50090-6027-1 | 50090602701 | 90 TABLET in 1 BOTTLE (50090-6027-1) | 90 tablet | 2022-06-30 | 0000-00-00 | No | No | Current |