Ezetimibe
- Product NDC
- 0904-6664
- 11-digit product format
- 009046664
- Labeler code
- 0904
- Product ID
- 0904-6664_4ff6c94b-7eb2-41e2-b404-01ff63cf27a4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ezetimibe
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA208332
- Marketing category
- ANDA
- Marketing start
- 2017-06-12
- Marketing end
- 2022-04-30
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0904-6664-04 | 00904666404 | 30 BLISTER PACK in 1 CARTON (0904-6664-04) > 1 TABLET in 1 BLISTER PACK | 30 blister pack | 2017-06-12 | 0000-00-00 | No | No | Current |