ESZOPICLONE
- Product NDC
- 71335-0005
- 11-digit product format
- 713350005
- Labeler code
- 71335
- Product ID
- 71335-0005_ccd3b5a4-e541-4e39-947a-749c06994d4e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ESZOPICLONE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA091113
- Marketing category
- ANDA
- Marketing start
- 2014-09-25
- Marketing end
- 0000-00-00
- Substance
- ESZOPICLONE
- Active strength
- 1 mg/1
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 71335-0005-1 | 71335000501 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-0005-1) | 2017-09-21 | 0000-00-00 | No | No | Current |
| 71335-0005-2 | 71335000502 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-0005-2) | 2017-09-21 | 0000-00-00 | No | No | Current |
| 71335-0005-3 | 71335000503 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-0005-3) | 2017-09-21 | 0000-00-00 | No | No | Current |
| 71335-0005-4 | 71335000504 | 10 TABLET, FILM COATED in 1 BOTTLE (71335-0005-4) | 2017-09-21 | 0000-00-00 | No | No | Current |
| 71335-0005-5 | 71335000505 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-0005-5) | 2017-09-21 | 0000-00-00 | No | No | Current |
| 71335-0005-6 | 71335000506 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-0005-6) | 2017-09-21 | 0000-00-00 | No | No | Current |