Olmesartan Medoxomil
- Product NDC
- 50090-7810
- 11-digit product format
- 500907810
- Labeler code
- 50090
- Product ID
- 50090-7810_7ae068de-8c92-4496-b691-88a8876662bc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Olmesartan Medoxomil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA203281
- Marketing category
- ANDA
- Marketing start
- 2017-05-25
- 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 |
|---|
| 50090-7810-0 | Olmesartan Medoxomil | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | | 3 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-7810-0 | 50090781000 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-7810-0) | 2025-12-05 | No | No | Historical |