OLMESARTAN MEDOXOMIL
- Product NDC
- 71335-2605
- 11-digit product format
- 713352605
- Labeler code
- 71335
- Product ID
- 71335-2605_cdbf03e1-b112-4e6c-b53d-09e678f09fdb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- olmesartan medoxomil
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA206720
- Marketing category
- ANDA
- Marketing start
- 2022-03-04
- 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
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- OLMESARTAN MEDOXOMIL
- Listing expiration
- 2027-12-31
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 |
|---|
| 71335-2605-1 | OLMESARTAN MEDOXOMIL | 30 in 1 BOTTLE | TABLET | 30 | | 100 |
| 71335-2605-2 | OLMESARTAN MEDOXOMIL | 90 in 1 BOTTLE | TABLET | 90 | | 100 |
| 71335-2605-3 | OLMESARTAN MEDOXOMIL | 28 in 1 BOTTLE | TABLET | 28 | | 100 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2605-1 | 71335260501 | 30 TABLET in 1 BOTTLE (71335-2605-1) | 30 tablet | 2026-03-12 | No | No | Historical |
| 71335-2605-2 | 71335260502 | 90 TABLET in 1 BOTTLE (71335-2605-2) | 90 tablet | 2026-03-12 | No | No | Historical |
| 71335-2605-3 | 71335260503 | 28 TABLET in 1 BOTTLE (71335-2605-3) | 28 tablet | 2026-03-12 | No | No | Historical |