Etodolac - 54868-4388-0 - (Etodolac)

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Drug Information of Etodolac

Product NDC: 54868-4388
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: 54868-4388
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075665
Marketing Category: ANDA
Start Marketing Date: 20110913

Package Information of Etodolac

Package NDC: 54868-4388-0
Package Description: 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (54868-4388-0)

NDC Information of Etodolac

NDC Code 54868-4388-0
Proprietary Name Etodolac
Package Description 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (54868-4388-0)
Product NDC 54868-4388
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Etodolac
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20110913
Marketing Category Name ANDA
Labeler Name Physicians Total Care, 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


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