Etodolac - 49349-019-02 - (Etodolac)

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Drug Information of Etodolac

Product NDC: 49349-019
Proprietary Name: Etodolac
Non Proprietary Name: Etodolac
Active Ingredient(s): 300    mg/1 & nbsp;   Etodolac
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Etodolac

Product NDC: 49349-019
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075419
Marketing Category: ANDA
Start Marketing Date: 20101006

Package Information of Etodolac

Package NDC: 49349-019-02
Package Description: 30 CAPSULE in 1 BLISTER PACK (49349-019-02)

NDC Information of Etodolac

NDC Code 49349-019-02
Proprietary Name Etodolac
Package Description 30 CAPSULE in 1 BLISTER PACK (49349-019-02)
Product NDC 49349-019
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Etodolac
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20101006
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name ETODOLAC
Strength Number 300
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