Olmesartan Medoxomil and Hydrochlorothiazide
- Product NDC
- 70756-812
- 11-digit product format
- 707560812
- Labeler code
- 70756
- Product ID
- 70756-812_45806c19-480f-987e-e063-6394a90aa8fa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Olmesartan Medoxomil and Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lifestar Pharma LLC
- Application
- ANDA208847
- Marketing category
- ANDA
- Marketing start
- 2020-10-01
- Substance
- HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL
- Active strength
- 12.5; 20 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Olmesartan Medoxomil and Hydrochlorothiazide
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| HYDROCHLOROTHIAZIDE | 12.5 mg/1 |
| OLMESARTAN MEDOXOMIL | 20 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 6M97XTV3HD, 0J48LPH2TH |
| Rxcui | 403853, 403854, 403855 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70756-812-12 | Olmesartan Medoxomil and Hydrochlorothiazide | 1000 in 1 BOTTLE | TABLET | 1000 | | 19 |
| 70756-812-30 | Olmesartan Medoxomil and Hydrochlorothiazide | 30 in 1 BOTTLE | TABLET | 30 | | 19 |
| 70756-812-51 | Olmesartan Medoxomil and Hydrochlorothiazide | 500 in 1 BOTTLE | TABLET | 500 | | 19 |
| 70756-812-90 | Olmesartan Medoxomil and Hydrochlorothiazide | 90 in 1 BOTTLE | TABLET | 90 | | 19 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70756-812 | OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE (OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE) TABLET [LIFESTAR PHARMA LLC] | 17 | Current NDC, Legacy NDC, 4 package rows | 20241225_9771066e-c05d-6a93-e053-2995a90a7e87.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70756-812-12 | 70756081212 | 1000 TABLET in 1 BOTTLE (70756-812-12) | 1000 tablet | 2020-10-01 | 0000-00-00 | No | No | Current |
| 70756-812-30 | 70756081230 | 30 TABLET in 1 BOTTLE (70756-812-30) | 30 tablet | 2020-10-01 | 0000-00-00 | No | No | Current |
| 70756-812-51 | 70756081251 | 500 TABLET in 1 BOTTLE (70756-812-51) | 500 tablet | 2020-10-01 | | No | No | Current |
| 70756-812-90 | 70756081290 | 90 TABLET in 1 BOTTLE (70756-812-90) | 90 tablet | 2020-10-01 | 0000-00-00 | No | No | Current |