Etodolac - 35356-324-60 - (Etodolac)

Alphabetical Index


Drug Information of Etodolac

Product NDC: 35356-324
Proprietary Name: Etodolac
Non Proprietary Name: Etodolac
Active Ingredient(s): 500    mg/1 & nbsp;   Etodolac
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Etodolac

Product NDC: 35356-324
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076174
Marketing Category: ANDA
Start Marketing Date: 20120306

Package Information of Etodolac

Package NDC: 35356-324-60
Package Description: 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (35356-324-60)

NDC Information of Etodolac

NDC Code 35356-324-60
Proprietary Name Etodolac
Package Description 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (35356-324-60)
Product NDC 35356-324
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Etodolac
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20120306
Marketing Category Name ANDA
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Substance Name ETODOLAC
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]

Complete Information of Etodolac


General Information