Eszopiclone
- Product NDC
- 50090-2606
- 11-digit product format
- 500902606
- Labeler code
- 50090
- Product ID
- 50090-2606_043494da-9882-4c60-830b-eff741b43134
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- eszopiclone
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA091151
- Marketing category
- ANDA
- Marketing start
- 2013-03-26
- Marketing end
- 0000-00-00
- Substance
- ESZOPICLONE
- Active strength
- 1 mg/1
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-2606-0 | Eszopiclone | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 8 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-2606 | ESZOPICLONE TABLET, FILM COATED [A-S MEDICATION SOLUTIONS] | 8 | Legacy NDC, 1 package rows | 20190114_641bf662-92f4-4aca-adf3-1e07718844f7.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50090-2606-0 | 50090260600 | 30 in 1 BOTTLE | Historical |