SULINDAC - 53489-479-10 - (sulindac)

Alphabetical Index


Drug Information of SULINDAC

Product NDC: 53489-479
Proprietary Name: SULINDAC
Non Proprietary Name: sulindac
Active Ingredient(s): 200    mg/1 & nbsp;   sulindac
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of SULINDAC

Product NDC: 53489-479
Labeler Name: Mutual Pharmaceutical Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA072051
Marketing Category: ANDA
Start Marketing Date: 20090904

Package Information of SULINDAC

Package NDC: 53489-479-10
Package Description: 1000 TABLET in 1 BOTTLE, PLASTIC (53489-479-10)

NDC Information of SULINDAC

NDC Code 53489-479-10
Proprietary Name SULINDAC
Package Description 1000 TABLET in 1 BOTTLE, PLASTIC (53489-479-10)
Product NDC 53489-479
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name sulindac
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090904
Marketing Category Name ANDA
Labeler Name Mutual Pharmaceutical Company, Inc.
Substance Name SULINDAC
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 SULINDAC


General Information