ESZOPICLONE
- Product NDC
- 63187-665
- 11-digit product format
- 631870665
- Labeler code
- 63187
- Product ID
- 63187-665_bbd1d1c9-8b2d-4b42-b7b3-b82bebfbf578
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ESZOPICLONE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA091113
- Marketing category
- ANDA
- Marketing start
- 2014-09-25
- 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63187-665 | ESZOPICLONE TABLET, FILM COATED [PROFICIENT RX LP] | 3 | Legacy NDC | 20191121_844c9558-bd34-4d8e-96bb-e022199ccc0d.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63187-665-30 | 63187066530 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (63187-665-30) | 2018-12-01 | 0000-00-00 | No | No | Current |
| 63187-665-60 | 63187066560 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (63187-665-60) | 2018-12-01 | 0000-00-00 | No | No | Current |
| 63187-665-90 | 63187066590 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (63187-665-90) | 2018-12-01 | 0000-00-00 | No | No | Current |