eszopiclone
- Product NDC
- 71335-0784
- 11-digit product format
- 713350784
- Labeler code
- 71335
- Product ID
- 71335-0784_a981accd-98a3-46e2-8669-c5b0739e6ed4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- eszopiclone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA091153
- Marketing category
- ANDA
- Marketing start
- 2014-04-15
- Marketing end
- 0000-00-00
- Substance
- ESZOPICLONE
- Active strength
- 3 mg/1
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-0784-1 | 71335078401 | 30 TABLET in 1 BOTTLE (71335-0784-1) | 30 tablet | 2014-04-25 | 0000-00-00 | No | No | Current |
| 71335-0784-2 | 71335078402 | 60 TABLET in 1 BOTTLE (71335-0784-2) | 60 tablet | 2014-04-25 | 0000-00-00 | No | No | Current |
| 71335-0784-3 | 71335078403 | 90 TABLET in 1 BOTTLE (71335-0784-3) | 90 tablet | 2014-04-25 | 0000-00-00 | No | No | Current |
| 71335-0784-4 | 71335078404 | 120 TABLET in 1 BOTTLE (71335-0784-4) | 120 tablet | 2014-04-25 | 0000-00-00 | No | No | Current |
| 71335-0784-5 | 71335078405 | 20 TABLET in 1 BOTTLE (71335-0784-5) | 20 tablet | 2014-04-25 | 0000-00-00 | No | No | Current |
| 71335-0784-6 | 71335078406 | 28 TABLET in 1 BOTTLE (71335-0784-6) | 28 tablet | 2014-04-25 | 0000-00-00 | No | No | Current |
| 71335-0784-7 | 71335078407 | 15 TABLET in 1 BOTTLE (71335-0784-7) | 15 tablet | 2014-04-15 | 0000-00-00 | No | No | Current |
| 71335-0784-8 | 71335078408 | 100 TABLET in 1 BOTTLE (71335-0784-8) | 100 tablet | 2014-04-25 | 0000-00-00 | No | No | Current |