Ezetimibe
- Product NDC
- 70518-1783
- 11-digit product format
- 705181783
- Labeler code
- 70518
- Product ID
- 70518-1783_7f2202ce-e5ea-1b15-e053-2a91aa0aaa46
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ezetimibe
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA209234
- Marketing category
- ANDA
- Marketing start
- 2019-01-09
- 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