Lunesta
- Product NDC
- 63629-3142
- 11-digit product format
- 636293142
- Labeler code
- 63629
- Product ID
- 63629-3142_ca386c45-4609-4bff-9bab-bdf0b879a7e4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ESZOPICLONE
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- NDA021476
- Marketing category
- NDA
- Marketing start
- 2005-04-04
- Marketing end
- 0000-00-00
- Substance
- ESZOPICLONE
- Active strength
- 3 mg/1
- DEA schedule
- CIV
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#