Olmesartan Medoxomil
- Product NDC
- 71335-2749
- 11-digit product format
- 713352749
- Labeler code
- 71335
- Product ID
- 71335-2749_07df4b70-92b1-4b8b-a912-b22997c14f0d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Olmesartan Medoxomil
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA206763
- Marketing category
- ANDA
- Marketing start
- 2017-04-24
- Substance
- OLMESARTAN MEDOXOMIL
- Active strength
- 40 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 | 40 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 6M97XTV3HD |
| Rxcui | 349405 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71335-2749-1 | Olmesartan Medoxomil | 30 in 1 BOTTLE | TABLET, COATED | 30 | | 1 |
| 71335-2749-2 | Olmesartan Medoxomil | 90 in 1 BOTTLE | TABLET, COATED | 90 | | 1 |
| 71335-2749-3 | Olmesartan Medoxomil | 28 in 1 BOTTLE | TABLET, COATED | 28 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2749-1 | 71335274901 | 30 TABLET, COATED in 1 BOTTLE (71335-2749-1) | 2025-10-03 | No | No | Historical |
| 71335-2749-2 | 71335274902 | 90 TABLET, COATED in 1 BOTTLE (71335-2749-2) | 2025-10-03 | No | No | Historical |
| 71335-2749-3 | 71335274903 | 28 TABLET, COATED in 1 BOTTLE (71335-2749-3) | 2025-10-03 | No | No | Historical |