ESZOPICLONE
- Product NDC
- 61919-323
- 11-digit product format
- 619190323
- Labeler code
- 61919
- Product ID
- 61919-323_2b19cbaf-7af0-45a7-bfff-5cdc41ba8dfb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ESZOPICLONE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- DirectRX
- Application
- ANDA091113
- Marketing category
- ANDA
- Marketing start
- 2015-01-01
- Marketing end
- 0000-00-00
- Substance
- ESZOPICLONE
- Active strength
- 1 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 |
|---|
| 61919-323-30 | ESZOPICLONE | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61919-323 | ESZOPICLONE TABLET, FILM COATED [DIRECTRX] | 1 | Legacy NDC, 1 package rows | 20151112_d483bd4d-f6ff-4942-94cc-00ed9655c29e.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 61919-323-30 | 61919032330 | 30 in 1 BOTTLE | Historical |