Lunesta - 49999-737-14 - (ESZOPICLONE)

Alphabetical Index


Drug Information of Lunesta

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)

Labeler Information of Lunesta

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 Information of Lunesta

Package NDC: 49999-737-14
Package Description: 14 TABLET, COATED in 1 BOTTLE, PLASTIC (49999-737-14)

NDC Information of Lunesta

NDC Code 49999-737-14
Proprietary Name Lunesta
Package Description 14 TABLET, COATED in 1 BOTTLE, PLASTIC (49999-737-14)
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

Complete Information of Lunesta


General Information