Ezetimibe
- Product NDC
- 60505-2945
- 11-digit product format
- 605052945
- Labeler code
- 60505
- Product ID
- 60505-2945_cf3d40b1-46f0-cd82-d6ce-fd8478e31f1a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ezetimibe
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Apotex Corp.
- Application
- ANDA208332
- Marketing category
- ANDA
- Marketing start
- 2017-06-12
- 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
- 2021-12-31
- 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 |
|---|
| 60505-2945-0 | 60505294500 | 10 BLISTER PACK in 1 CARTON (60505-2945-0) > 10 TABLET in 1 BLISTER PACK | 10 blister pack | 2017-06-12 | 0000-00-00 | No | No | Current |
| 60505-2945-1 | 60505294501 | 100 TABLET in 1 BOTTLE (60505-2945-1) | 100 tablet | 2017-06-12 | 0000-00-00 | No | No | Current |
| 60505-2945-3 | 60505294503 | 30 TABLET in 1 BOTTLE (60505-2945-3) | 30 tablet | 2017-06-12 | 0000-00-00 | No | No | Current |
| 60505-2945-5 | 60505294505 | 500 TABLET in 1 BOTTLE (60505-2945-5) | 500 tablet | 2017-06-12 | 0000-00-00 | No | No | Current |
| 60505-2945-8 | 60505294508 | 1000 TABLET in 1 BOTTLE (60505-2945-8) | 1000 tablet | 2017-06-12 | 0000-00-00 | No | No | Current |
| 60505-2945-9 | 60505294509 | 90 TABLET in 1 BOTTLE (60505-2945-9) | 90 tablet | 2017-06-12 | 0000-00-00 | No | No | Current |