Product NDC: | 54868-5394 |
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: | 54868-5394 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021476 |
Marketing Category: | NDA |
Start Marketing Date: | 20050824 |
Package NDC: | 54868-5394-0 |
Package Description: | 10 TABLET, COATED in 1 BOTTLE, PLASTIC (54868-5394-0) |
NDC Code | 54868-5394-0 |
Proprietary Name | Lunesta |
Package Description | 10 TABLET, COATED in 1 BOTTLE, PLASTIC (54868-5394-0) |
Product NDC | 54868-5394 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | ESZOPICLONE |
Dosage Form Name | TABLET, COATED |
Route Name | ORAL |
Start Marketing Date | 20050824 |
Marketing Category Name | NDA |
Labeler Name | Physicians Total Care, Inc. |
Substance Name | ESZOPICLONE |
Strength Number | 3 |
Strength Unit | mg/1 |
Pharmaceutical Classes |