Etodolac - 51672-4052-3 - (Etodolac)

Alphabetical Index


Drug Information of Etodolac

Product NDC: 51672-4052
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: 51672-4052
Labeler Name: Taro Pharmaceuticals U.S.A., Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076174
Marketing Category: ANDA
Start Marketing Date: 20030313

Package Information of Etodolac

Package NDC: 51672-4052-3
Package Description: 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (51672-4052-3)

NDC Information of Etodolac

NDC Code 51672-4052-3
Proprietary Name Etodolac
Package Description 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (51672-4052-3)
Product NDC 51672-4052
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Etodolac
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20030313
Marketing Category Name ANDA
Labeler Name Taro Pharmaceuticals U.S.A., Inc.
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