eszopiclone
- Product NDC
- 63187-330
- 11-digit product format
- 631870330
- Labeler code
- 63187
- Product ID
- 63187-330_53838253-c007-41ac-b7a9-0c817eb73fd5
- 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
- 2 mg/1
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record