Etodolac - 60505-0102-2 - (Etodolac)

Alphabetical Index


Drug Information of Etodolac

Product NDC: 60505-0102
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: 60505-0102
Labeler Name: Apotex Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076004
Marketing Category: ANDA
Start Marketing Date: 20030501

Package Information of Etodolac

Package NDC: 60505-0102-2
Package Description: 500 TABLET, FILM COATED in 1 BOTTLE (60505-0102-2)

NDC Information of Etodolac

NDC Code 60505-0102-2
Proprietary Name Etodolac
Package Description 500 TABLET, FILM COATED in 1 BOTTLE (60505-0102-2)
Product NDC 60505-0102
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Etodolac
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20030501
Marketing Category Name ANDA
Labeler Name Apotex Corp.
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