Sulindac - 54738-902-02 - (Sulindac)

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Drug Information of Sulindac

Product NDC: 54738-902
Proprietary Name: Sulindac
Non Proprietary Name: Sulindac
Active Ingredient(s): 150    mg/1 & nbsp;   Sulindac
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Sulindac

Product NDC: 54738-902
Labeler Name: Richmond Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA072050
Marketing Category: ANDA
Start Marketing Date: 20090904

Package Information of Sulindac

Package NDC: 54738-902-02
Package Description: 500 TABLET in 1 BOTTLE, PLASTIC (54738-902-02)

NDC Information of Sulindac

NDC Code 54738-902-02
Proprietary Name Sulindac
Package Description 500 TABLET in 1 BOTTLE, PLASTIC (54738-902-02)
Product NDC 54738-902
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 Richmond Pharmaceuticals
Substance Name SULINDAC
Strength Number 150
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