Etodolac - 49349-020-02 - (Etodolac)

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Drug Information of Etodolac

Product NDC: 49349-020
Proprietary Name: Etodolac
Non Proprietary Name: Etodolac
Active Ingredient(s): 400    mg/1 & nbsp;   Etodolac
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Etodolac

Product NDC: 49349-020
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074839
Marketing Category: ANDA
Start Marketing Date: 20101001

Package Information of Etodolac

Package NDC: 49349-020-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-020-02)

NDC Information of Etodolac

NDC Code 49349-020-02
Proprietary Name Etodolac
Package Description 30 TABLET in 1 BLISTER PACK (49349-020-02)
Product NDC 49349-020
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Etodolac
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20101001
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name ETODOLAC
Strength Number 400
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