Eszopiclone
- Product NDC
- 68788-8077
- 11-digit product format
- 687888077
- Labeler code
- 68788
- Product ID
- 68788-8077_f0e32629-c180-4bd5-9c05-38bf254a0049
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Eszopiclone
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc. USA
- Application
- ANDA091166
- Marketing category
- ANDA
- Marketing start
- 2021-09-03
- Marketing end
- 0000-00-00
- Substance
- ESZOPICLONE
- Active strength
- 2 mg/1
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68788-8077 | ESZOPICLONE TABLET, FILM COATED [PREFERRED PHARMACEUTICALS INC. USA] | 5 | Legacy NDC | 20250504_f924836c-bf05-4d7e-b448-bb189a46045b.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-8077-3 | 68788807703 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-8077-3) | 2021-09-03 | 0000-00-00 | No | No | Current |
| 68788-8077-6 | 68788807706 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-8077-6) | 2021-09-03 | 0000-00-00 | No | No | Current |
| 68788-8077-9 | 68788807709 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-8077-9) | 2021-09-03 | 0000-00-00 | No | No | Current |