Product NDC: | 49999-737 |
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) |
Product NDC: | 49999-737 |
Labeler Name: | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021476 |
Marketing Category: | NDA |
Start Marketing Date: | 20110718 |
Package NDC: | 49999-737-90 |
Package Description: | 90 TABLET, COATED in 1 BOTTLE, PLASTIC (49999-737-90) |
NDC Code | 49999-737-90 |
Proprietary Name | Lunesta |
Package Description | 90 TABLET, COATED in 1 BOTTLE, PLASTIC (49999-737-90) |
Product NDC | 49999-737 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | ESZOPICLONE |
Dosage Form Name | TABLET, COATED |
Route Name | ORAL |
Start Marketing Date | 20110718 |
Marketing Category Name | NDA |
Labeler Name | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC |
Substance Name | ESZOPICLONE |
Strength Number | 3 |
Strength Unit | mg/1 |
Pharmaceutical Classes |