Ezetimibe
- Product NDC
- 71335-1354
- 11-digit product format
- 713351354
- Labeler code
- 71335
- Product ID
- 71335-1354_4d1e98fc-f35e-46be-86f5-d18334971339
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ezetimibe
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- 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
- 2020-12-31
- 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 |
|---|
| 71335-1354-1 | 71335135401 | 30 TABLET in 1 BOTTLE (71335-1354-1) | 30 tablet | 2019-09-27 | 0000-00-00 | No | No | Current |
| 71335-1354-2 | 71335135402 | 90 TABLET in 1 BOTTLE (71335-1354-2) | 90 tablet | 2019-09-27 | 0000-00-00 | No | No | Current |
| 71335-1354-3 | 71335135403 | 28 TABLET in 1 BOTTLE (71335-1354-3) | 28 tablet | 2019-09-27 | 0000-00-00 | No | No | Current |
| 71335-1354-4 | 71335135404 | 18 TABLET in 1 BOTTLE (71335-1354-4) | 18 tablet | 2019-09-27 | 0000-00-00 | No | No | Current |
| 71335-1354-5 | 71335135405 | 60 TABLET in 1 BOTTLE (71335-1354-5) | 60 tablet | 2019-09-27 | 0000-00-00 | No | No | Current |