Etodolac - 68788-9929-2 - (Etodolac)

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Drug Information of Etodolac

Product NDC: 68788-9929
Proprietary Name: Etodolac
Non Proprietary Name: Etodolac
Active Ingredient(s): 400    mg/1 & nbsp;   Etodolac
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Etodolac

Product NDC: 68788-9929
Labeler Name: Preferred Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075074
Marketing Category: ANDA
Start Marketing Date: 20120117

Package Information of Etodolac

Package NDC: 68788-9929-2
Package Description: 20 TABLET, FILM COATED in 1 BOTTLE (68788-9929-2)

NDC Information of Etodolac

NDC Code 68788-9929-2
Proprietary Name Etodolac
Package Description 20 TABLET, FILM COATED in 1 BOTTLE (68788-9929-2)
Product NDC 68788-9929
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Etodolac
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120117
Marketing Category Name ANDA
Labeler Name Preferred 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