Eszopiclone
- Product NDC
- 71335-2698
- 11-digit product format
- 713352698
- Labeler code
- 71335
- Product ID
- 71335-2698_acb17086-1db0-4e39-826b-45ca84eb73d8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Eszopiclone
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA202929
- Marketing category
- ANDA
- Marketing start
- 2015-01-31
- Substance
- ESZOPICLONE
- Active strength
- 2 mg/1
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Eszopiclone
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ESZOPICLONE | 2 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | UZX80K71OE |
| Rxcui | 485442 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71335-2698-1 | Eszopiclone | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 1 |
| 71335-2698-2 | Eszopiclone | 60 in 1 BOTTLE | TABLET, FILM COATED | 60 | | 1 |
| 71335-2698-3 | Eszopiclone | 28 in 1 BOTTLE | TABLET, FILM COATED | 28 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2698-1 | 71335269801 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-2698-1) | 2025-09-24 | No | No | Historical |
| 71335-2698-2 | 71335269802 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-2698-2) | 2025-09-24 | No | No | Historical |
| 71335-2698-3 | 71335269803 | 28 TABLET, FILM COATED in 1 BOTTLE (71335-2698-3) | 2025-09-24 | No | No | Historical |