eszopiclone
- Product NDC
- 68788-9238
- 11-digit product format
- 687889238
- Labeler code
- 68788
- Product ID
- 68788-9238_13523811-1905-4c59-a33e-c71334f699a0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- eszopiclone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA091153
- Marketing category
- ANDA
- Marketing start
- 2014-10-13
- Marketing end
- 0000-00-00
- Substance
- ESZOPICLONE
- Active strength
- 3 mg/1
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record