OLMESARTAN MEDOXOMIL
- Product NDC
- 50090-7680
- 11-digit product format
- 500907680
- Labeler code
- 50090
- Product ID
- 50090-7680_59bc6fc7-ac1c-4b5c-987e-9212ae532d28
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Olmesartan medoxomil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA211049
- Marketing category
- ANDA
- Marketing start
- 2019-03-05
- 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 |
|---|
| 50090-7680-0 | OLMESARTAN MEDOXOMIL | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 2 |
| 50090-7680-1 | OLMESARTAN MEDOXOMIL | 90 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 90 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-7680-0 | 50090768000 | 30 TABLET, FILM COATED in 1 BOTTLE (50090-7680-0) | 2025-10-09 | No | No | Current |
| 50090-7680-1 | 50090768001 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-7680-1) | 2025-10-09 | No | No | Current |