Eszopiclone
- Product NDC
- 68788-8923
- 11-digit product format
- 687888923
- Labeler code
- 68788
- Product ID
- 68788-8923_d858371a-33e6-4ce8-a51c-b88ff3ac8b9e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Eszopiclone
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA091166
- Marketing category
- ANDA
- Marketing start
- 2015-10-06
- Marketing end
- 0000-00-00
- Substance
- ESZOPICLONE
- Active strength
- 2 mg/1
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record