Lunesta
- Product NDC
- 50436-0193
- 11-digit product format
- 504360193
- Labeler code
- 50436
- Product ID
- 50436-0193_43f0f104-7592-444b-a118-13c2e848f74f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ESZOPICLONE
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- NDA021476
- Marketing category
- NDA
- Marketing start
- 2005-04-04
- Marketing end
- 0000-00-00
- Substance
- ESZOPICLONE
- Active strength
- 3 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 50436-0193-1 | EA - Each | 50436-0193 | df206a23-e518-4901-94cf-a68cc8669fc0 | 1 | 2012-07-24 |