Lunesta
- Product NDC
- 68258-7048
- 11-digit product format
- 682587048
- Labeler code
- 68258
- Product ID
- 68258-7048_abf41383-30a2-43ec-b4d3-1c17836b8900
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ESZOPICLONE
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Dispensing Solutions, Inc.
- Application
- NDA021476
- Marketing category
- NDA
- Marketing start
- 2005-04-04
- Marketing end
- 0000-00-00
- Substance
- ESZOPICLONE
- Active strength
- 2 mg/1
- DEA schedule
- CIV
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 68258-7048-3 | Lunesta | 30 in 1 BOTTLE | TABLET, COATED | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68258-7048 | LUNESTA (ESZOPICLONE) TABLET, COATED [DISPENSING SOLUTIONS, INC.] | 1 | Legacy NDC, 1 package rows | 20111013_20b122fb-42ec-4fa1-9a9e-e5930e5d2e7e.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 68258-7048-3 | 68258704803 | 30 in 1 BOTTLE | Historical |