Ezetimibe
- Product NDC
- 50090-7236
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ezetimibe
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA209234
- Marketing category
- ANDA
- Substance
- EZETIMIBE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 50090-7236-0 | 90 TABLET in 1 BOTTLE (50090-7236-0) | 2024-08-28 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Ezetimibe | A-S Medication Solutions | 2025-10-10 | Human Prescription Drug Label | 2 |