Etodolac - 51672-4036-1 - (Etodolac)

Alphabetical Index


Drug Information of Etodolac

Product NDC: 51672-4036
Proprietary Name: Etodolac
Non Proprietary Name: Etodolac
Active Ingredient(s): 500    mg/1 & nbsp;   Etodolac
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Etodolac

Product NDC: 51672-4036
Labeler Name: Taro Pharmaceuticals U.S.A., Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075074
Marketing Category: ANDA
Start Marketing Date: 20000425

Package Information of Etodolac

Package NDC: 51672-4036-1
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE (51672-4036-1)

NDC Information of Etodolac

NDC Code 51672-4036-1
Proprietary Name Etodolac
Package Description 100 TABLET, FILM COATED in 1 BOTTLE (51672-4036-1)
Product NDC 51672-4036
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Etodolac
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20000425
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