EZETIMIBE
- Product NDC
- 72189-118
- 11-digit product format
- 721890118
- Labeler code
- 72189
- Product ID
- 72189-118_e9d5b283-094e-393f-e053-2995a90a930c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- EZETIMIBE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- direct rx
- Application
- ANDA209234
- Marketing category
- ANDA
- Marketing start
- 2020-12-02
- Marketing end
- 0000-00-00
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72189-118-30 | EZETIMIBE | 30 in 1 BOTTLE | TABLET | 30 | | 2 |
| 72189-118-90 | EZETIMIBE | 90 in 1 BOTTLE | TABLET | 90 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72189-118 | EZETIMIBE TABLET [DIRECT RX] | 2 | Legacy NDC, 2 package rows | 20220930_b57dcdef-894c-4801-e053-2a95a90a7239.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72189-118-30 | 72189011830 | 30 TABLET in 1 BOTTLE (72189-118-30) | 30 tablet | 2020-12-02 | 0000-00-00 | No | No | Current |
| 72189-118-90 | 72189011890 | 90 TABLET in 1 BOTTLE (72189-118-90) | 90 tablet | 2020-12-02 | 0000-00-00 | No | No | Current |