Etodolac - 51672-4017-1 - (Etodolac)

Alphabetical Index


Drug Information of Etodolac

Product NDC: 51672-4017
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: 51672-4017
Labeler Name: Taro Pharmaceuticals U.S.A., Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075078
Marketing Category: ANDA
Start Marketing Date: 19980430

Package Information of Etodolac

Package NDC: 51672-4017-1
Package Description: 100 CAPSULE in 1 BOTTLE (51672-4017-1)

NDC Information of Etodolac

NDC Code 51672-4017-1
Proprietary Name Etodolac
Package Description 100 CAPSULE in 1 BOTTLE (51672-4017-1)
Product NDC 51672-4017
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Etodolac
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19980430
Marketing Category Name ANDA
Labeler Name Taro Pharmaceuticals U.S.A., 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