EZETIMIBE
- Product NDC
- 50090-7689
- 11-digit product format
- 500907689
- Labeler code
- 50090
- Product ID
- 50090-7689_fbc0bed9-2a61-4400-867d-442488449348
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- EZETIMIBE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA210859
- Marketing category
- ANDA
- Marketing start
- 2022-07-26
- Substance
- EZETIMIBE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Decreased Cholesterol Absorption [PE], Dietary Cholesterol Absorption Inhibitor [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- EZETIMIBE
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| EZETIMIBE | 10 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | EOR26LQQ24 |
| Rxcui | 349556 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-7689-0 | EZETIMIBE | 90 in 1 BOTTLE | TABLET | 90 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-7689-0 | 50090768900 | 90 TABLET in 1 BOTTLE (50090-7689-0) | 90 tablet | 2025-10-10 | No | No | Current |