Eszopiclone
- Product NDC
- 68788-6953
- 11-digit product format
- 687886953
- Labeler code
- 68788
- Product ID
- 68788-6953_10ead623-c81b-4ff1-9079-7c53e5ba2555
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Eszopiclone
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA202929
- Marketing category
- ANDA
- Marketing start
- 2017-05-01
- Marketing end
- 0000-00-00
- Substance
- ESZOPICLONE
- Active strength
- 1 mg/1
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-6953-0 | 68788695300 | 100 TABLET, FILM COATED in 1 BOTTLE (68788-6953-0) | 2017-05-01 | 0000-00-00 | No | No | Current |
| 68788-6953-1 | 68788695301 | 10 TABLET, FILM COATED in 1 BOTTLE (68788-6953-1) | 2017-05-01 | 0000-00-00 | No | No | Current |
| 68788-6953-2 | 68788695302 | 20 TABLET, FILM COATED in 1 BOTTLE (68788-6953-2) | 2017-05-01 | 0000-00-00 | No | No | Current |
| 68788-6953-3 | 68788695303 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-6953-3) | 2017-05-01 | 0000-00-00 | No | No | Current |
| 68788-6953-5 | 68788695305 | 15 TABLET, FILM COATED in 1 BOTTLE (68788-6953-5) | 2017-05-01 | 0000-00-00 | No | No | Current |
| 68788-6953-6 | 68788695306 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-6953-6) | 2017-05-01 | 0000-00-00 | No | No | Current |
| 68788-6953-7 | 68788695307 | 7 TABLET, FILM COATED in 1 BOTTLE (68788-6953-7) | 2017-05-01 | 0000-00-00 | No | No | Current |
| 68788-6953-9 | 68788695309 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-6953-9) | 2017-05-01 | 0000-00-00 | No | No | Current |