Olmesartan Medoxomil
- Product NDC
- 72241-079
- 11-digit product format
- 722410079
- Labeler code
- 72241
- Product ID
- 72241-079_1f430fc9-bd4c-4328-a4a2-501ec991029b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Olmesartan Medoxomil
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Modavar Pharmaceuticals LLC
- Application
- ANDA210682
- Marketing category
- ANDA
- Marketing start
- 2025-07-01
- Substance
- OLMESARTAN MEDOXOMIL
- Active strength
- 20 mg/1
- Pharmacologic classes
- Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC]
- 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
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| OLMESARTAN MEDOXOMIL | 20 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 6M97XTV3HD |
| Rxcui | 349373, 349401, 349405 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72241-079-04 | Olmesartan Medoxomil | 90 in 1 BOTTLE | TABLET, COATED | 90 | | 1 |
| 72241-079-10 | Olmesartan Medoxomil | 500 in 1 BOTTLE | TABLET, COATED | 500 | | 1 |
| 72241-079-22 | Olmesartan Medoxomil | 30 in 1 BOTTLE | TABLET, COATED | 30 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 72241-079-04 | 72241007904 | 90 TABLET, COATED in 1 BOTTLE (72241-079-04) | 2025-07-01 | No | No | Historical |
| 72241-079-10 | 72241007910 | 500 TABLET, COATED in 1 BOTTLE (72241-079-10) | 2025-07-01 | No | No | Historical |
| 72241-079-22 | 72241007922 | 30 TABLET, COATED in 1 BOTTLE (72241-079-22) | 2025-07-01 | No | No | Historical |