Eszopiclone
- Product NDC
- 70518-0816
- 11-digit product format
- 705180816
- Labeler code
- 70518
- Product ID
- 70518-0816_8ecf238e-248a-7e1b-e053-2a95a90a5ae5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Eszopiclone
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA091024
- Marketing category
- ANDA
- Marketing start
- 2017-11-02
- 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