OLMESARTAN MEDOXOMIL
- Product NDC
- 50090-7681
- 11-digit product format
- 500907681
- Labeler code
- 50090
- Product ID
- 50090-7681_14dd93c4-2a8d-41d7-b844-66b048ef7315
- 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
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 |
|---|
| 50090-7681-0 | 50090768100 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-7681-0) | 2025-10-09 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| OLMESARTAN MEDOXOMIL | A-S Medication Solutions | 2025-10-09 | HUMAN PRESCRIPTION DRUG LABEL | 1 |