Etodolac - 60429-315-01 - (Etodolac)

Alphabetical Index


Drug Information of Etodolac

Product NDC: 60429-315
Proprietary Name: Etodolac
Non Proprietary Name: Etodolac
Active Ingredient(s): 600    mg/1 & nbsp;   Etodolac
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Etodolac

Product NDC: 60429-315
Labeler Name: Golden State Medical Supply, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076174
Marketing Category: ANDA
Start Marketing Date: 20030313

Package Information of Etodolac

Package NDC: 60429-315-01
Package Description: 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (60429-315-01)

NDC Information of Etodolac

NDC Code 60429-315-01
Proprietary Name Etodolac
Package Description 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (60429-315-01)
Product NDC 60429-315
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Etodolac
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20030313
Marketing Category Name ANDA
Labeler Name Golden State Medical Supply, Inc.
Substance Name ETODOLAC
Strength Number 600
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