Etodolac - 54868-1852-1 - (Etodolac)

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Drug Information of Etodolac

Product NDC: 54868-1852
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, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Etodolac

Product NDC: 54868-1852
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075665
Marketing Category: ANDA
Start Marketing Date: 20050120

Package Information of Etodolac

Package NDC: 54868-1852-1
Package Description: 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (54868-1852-1)

NDC Information of Etodolac

NDC Code 54868-1852-1
Proprietary Name Etodolac
Package Description 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (54868-1852-1)
Product NDC 54868-1852
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Etodolac
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20050120
Marketing Category Name ANDA
Labeler Name Physicians Total Care, 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