Sulindac - 42806-011-05 - (Sulindac)

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Drug Information of Sulindac

Product NDC: 42806-011
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: 42806-011
Labeler Name: Epic Pharma, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA072711
Marketing Category: ANDA
Start Marketing Date: 20100125

Package Information of Sulindac

Package NDC: 42806-011-05
Package Description: 500 TABLET in 1 BOTTLE (42806-011-05)

NDC Information of Sulindac

NDC Code 42806-011-05
Proprietary Name Sulindac
Package Description 500 TABLET in 1 BOTTLE (42806-011-05)
Product NDC 42806-011
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Sulindac
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100125
Marketing Category Name ANDA
Labeler Name Epic Pharma, LLC
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