Sulindac - 55289-930-30 - (Sulindac)

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Drug Information of Sulindac

Product NDC: 55289-930
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: 55289-930
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071795
Marketing Category: ANDA
Start Marketing Date: 19900403

Package Information of Sulindac

Package NDC: 55289-930-30
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (55289-930-30)

NDC Information of Sulindac

NDC Code 55289-930-30
Proprietary Name Sulindac
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (55289-930-30)
Product NDC 55289-930
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 PD-Rx Pharmaceuticals, 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