OLMESARTAN MEDOXOMIL
- Product NDC
- 50090-7680
- 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
- Substance
- OLMESARTAN MEDOXOMIL
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 50090-7680-0 | 30 TABLET, FILM COATED in 1 BOTTLE (50090-7680-0) | 2025-10-09 | | No | Historical |
| 50090-7680-1 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-7680-1) | 2025-10-09 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| OLMESARTAN MEDOXOMIL | A-S Medication Solutions | 2025-10-09 | HUMAN PRESCRIPTION DRUG LABEL | 2 |