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Lunesta
Lunesta - 63629-3142-5 - (ESZOPICLONE)
Drug Information of Lunesta
| Product NDC: | 63629-3142 |
| Proprietary Name: | Lunesta |
| Non Proprietary Name: | ESZOPICLONE |
| Active Ingredient(s): | 3 mg/1 & nbsp; ESZOPICLONE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Lunesta
| Product NDC: | 63629-3142 |
| Labeler Name: | Bryant Ranch Prepack |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021476 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20050404 |
Package Information of Lunesta
| Package NDC: | 63629-3142-5 |
| Package Description: | 14 TABLET, COATED in 1 BOTTLE (63629-3142-5) |
NDC Information of Lunesta
| NDC Code | 63629-3142-5 |
| Proprietary Name | Lunesta |
| Package Description | 14 TABLET, COATED in 1 BOTTLE (63629-3142-5) |
| Product NDC | 63629-3142 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ESZOPICLONE |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20050404 |
| Marketing Category Name | NDA |
| Labeler Name | Bryant Ranch Prepack |
| Substance Name | ESZOPICLONE |
| Strength Number | 3 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
