Olmesartan Medoxomil
- Product NDC
- 71335-2362
- 11-digit product format
- 713352362
- Labeler code
- 71335
- Product ID
- 71335-2362_9c6c0024-b3a6-4126-9f25-923c7a00310e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Olmesartan Medoxomil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA204798
- 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 |
|---|
| OLMESARTAN MEDOXOMIL | 40 mg/1 |
Harmonized Identifiers
| Field | Values |
|---|
| Unii | 6M97XTV3HD |
| Rxcui | 349405 |
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 6M97XTV3HD | OLMESARTAN MEDOXOMIL | 144689-63-4 | OLMESARTAN MEDOXOMIL |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2362-1 | 71335236201 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-2362-1) | 2024-03-11 | No | No | Current |
| 71335-2362-2 | 71335236202 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-2362-2) | 2024-03-11 | No | No | Current |
| 71335-2362-3 | 71335236203 | 28 TABLET, FILM COATED in 1 BOTTLE (71335-2362-3) | 2024-05-30 | No | No | Current |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Olmesartan Medoxomil | Bryant Ranch Prepack | 2025-03-31 | HUMAN PRESCRIPTION DRUG LABEL | 102 |