Etodolac - 0228-2599-11 - (Etodolac)

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Drug Information of Etodolac

Product NDC: 0228-2599
Proprietary Name: Etodolac
Non Proprietary Name: Etodolac
Active Ingredient(s): 400    mg/1 & nbsp;   Etodolac
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Etodolac

Product NDC: 0228-2599
Labeler Name: Actavis Elizabeth LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074819
Marketing Category: ANDA
Start Marketing Date: 19970331

Package Information of Etodolac

Package NDC: 0228-2599-11
Package Description: 100 TABLET in 1 BOTTLE (0228-2599-11)

NDC Information of Etodolac

NDC Code 0228-2599-11
Proprietary Name Etodolac
Package Description 100 TABLET in 1 BOTTLE (0228-2599-11)
Product NDC 0228-2599
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Etodolac
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19970331
Marketing Category Name ANDA
Labeler Name Actavis Elizabeth LLC
Substance Name ETODOLAC
Strength Number 400
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