Sulindac - 53808-0303-1 - (SULINDAC)

Alphabetical Index


Drug Information of Sulindac

Product NDC: 53808-0303
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: 53808-0303
Labeler Name: State of Florida DOH Central Pharmacy
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA073262
Marketing Category: ANDA
Start Marketing Date: 20090701

Package Information of Sulindac

Package NDC: 53808-0303-1
Package Description: 30 TABLET in 1 BLISTER PACK (53808-0303-1)

NDC Information of Sulindac

NDC Code 53808-0303-1
Proprietary Name Sulindac
Package Description 30 TABLET in 1 BLISTER PACK (53808-0303-1)
Product NDC 53808-0303
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name SULINDAC
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090701
Marketing Category Name ANDA
Labeler Name State of Florida DOH Central Pharmacy
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