eszopiclone
- Product NDC
- 63187-365
- 11-digit product format
- 631870365
- Labeler code
- 63187
- Product ID
- 63187-365_d41272f9-2886-4b65-87a6-4bd5f01cabda
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- eszopiclone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA091153
- Marketing category
- ANDA
- Marketing start
- 2014-04-15
- Marketing end
- 0000-00-00
- Substance
- ESZOPICLONE
- Active strength
- 3 mg/1
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record