Etodolac - 55289-239-45 - (Etodolac)

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Drug Information of Etodolac

Product NDC: 55289-239
Proprietary Name: Etodolac
Non Proprietary Name: Etodolac
Active Ingredient(s): 400    mg/1 & nbsp;   Etodolac
Administration Route(s): ORAL
Dosage Form(s): TABLET, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Etodolac

Product NDC: 55289-239
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074903
Marketing Category: ANDA
Start Marketing Date: 19970411

Package Information of Etodolac

Package NDC: 55289-239-45
Package Description: 45 TABLET, COATED in 1 BOTTLE, PLASTIC (55289-239-45)

NDC Information of Etodolac

NDC Code 55289-239-45
Proprietary Name Etodolac
Package Description 45 TABLET, COATED in 1 BOTTLE, PLASTIC (55289-239-45)
Product NDC 55289-239
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Etodolac
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 19970411
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, 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