Eszopiclone
- Product NDC
- 50090-1748
- 11-digit product format
- 500901748
- Labeler code
- 50090
- Product ID
- 50090-1748_9ffc447a-2d89-487b-9b83-bb7b7229f7aa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Eszopiclone
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA091124
- Marketing category
- ANDA
- Marketing start
- 2014-04-15
- 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