OLMESARTAN MEDOXOMIL
- Product NDC
- 72189-137
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- OLMESARTAN MEDOXOMIL
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- direct rx
- Application
- ANDA207662
- Marketing category
- ANDA
- Substance
- OLMESARTAN MEDOXOMIL
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 72189-137-30 | 30 TABLET, FILM COATED in 1 BOTTLE (72189-137-30) | 2020-12-02 | | No | Historical |
| 72189-137-90 | 90 TABLET, FILM COATED in 1 BOTTLE (72189-137-90) | 2020-12-02 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| OLMESARTAN MEDOXOMIL | direct rx | 2025-01-17 | HUMAN PRESCRIPTION DRUG LABEL | 4 |