Sulindac - 63629-3208-2 - (Sulindac)

Alphabetical Index


Drug Information of Sulindac

Product NDC: 63629-3208
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: 63629-3208
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071795
Marketing Category: ANDA
Start Marketing Date: 19900403

Package Information of Sulindac

Package NDC: 63629-3208-2
Package Description: 60 TABLET in 1 BOTTLE (63629-3208-2)

NDC Information of Sulindac

NDC Code 63629-3208-2
Proprietary Name Sulindac
Package Description 60 TABLET in 1 BOTTLE (63629-3208-2)
Product NDC 63629-3208
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Sulindac
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19900403
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
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