Etodolac - 55289-418-30 - (Etodolac)

Alphabetical Index


Drug Information of Etodolac

Product NDC: 55289-418
Proprietary Name: Etodolac
Non Proprietary Name: Etodolac
Active Ingredient(s): 500    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: 55289-418
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074903
Marketing Category: ANDA
Start Marketing Date: 19990419

Package Information of Etodolac

Package NDC: 55289-418-30
Package Description: 30 TABLET, COATED in 1 BOTTLE, PLASTIC (55289-418-30)

NDC Information of Etodolac

NDC Code 55289-418-30
Proprietary Name Etodolac
Package Description 30 TABLET, COATED in 1 BOTTLE, PLASTIC (55289-418-30)
Product NDC 55289-418
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Etodolac
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 19990419
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, 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