Etodolac - 54868-5274-1 - (etodolac)

Alphabetical Index


Drug Information of Etodolac

Product NDC: 54868-5274
Proprietary Name: Etodolac
Non Proprietary Name: etodolac
Active Ingredient(s): 200    mg/1 & nbsp;   etodolac
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Etodolac

Product NDC: 54868-5274
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075078
Marketing Category: ANDA
Start Marketing Date: 20050427

Package Information of Etodolac

Package NDC: 54868-5274-1
Package Description: 20 CAPSULE in 1 BOTTLE (54868-5274-1)

NDC Information of Etodolac

NDC Code 54868-5274-1
Proprietary Name Etodolac
Package Description 20 CAPSULE in 1 BOTTLE (54868-5274-1)
Product NDC 54868-5274
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name etodolac
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20050427
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name ETODOLAC
Strength Number 200
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