Eszopiclone
- Product NDC
- 70518-2979
- 11-digit product format
- 705182979
- Labeler code
- 70518
- Product ID
- 70518-2979_d3d40a15-2e3b-50d5-e053-2a95a90a348e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Eszopiclone
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA091124
- Marketing category
- ANDA
- Marketing start
- 2020-12-29
- Marketing end
- 0000-00-00
- Substance
- ESZOPICLONE
- Active strength
- 3 mg/1
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2979-0 | 70518297900 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2979-0) | 2020-12-29 | 0000-00-00 | No | No | Current |