Ezetimibe
- Product NDC
- 70518-2262
- 11-digit product format
- 705182262
- Labeler code
- 70518
- Product ID
- 70518-2262_c78eff45-cb1e-f05f-e053-2a95a90a71f0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ezetimibe
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA209234
- Marketing category
- ANDA
- Marketing start
- 2019-08-12
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2262-0 | 70518226200 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-2262-0) | 90 tablet | 2019-08-12 | 0000-00-00 | No | No | Current |