Eszopiclone
- Product NDC
- 50090-3989
- 11-digit product format
- 500903989
- Labeler code
- 50090
- Product ID
- 50090-3989_35d7dbc4-ea07-4fee-87c5-e4bad735ce99
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Eszopiclone
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA091166
- Marketing category
- ANDA
- Marketing start
- 2014-04-15
- Marketing end
- 0000-00-00
- Substance
- ESZOPICLONE
- Active strength
- 1 mg/1
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| UZX80K71OE | ESZOPICLONE | 138729-47-2 | ESZOPICLONE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-3989-0 | 50090398900 | 30 TABLET, FILM COATED in 1 BOTTLE (50090-3989-0) | 2018-12-18 | 0000-00-00 | No | No | Current |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Eszopiclone | A-S Medication Solutions | 2019-01-02 | HUMAN PRESCRIPTION DRUG LABEL | 1 |