Sulindac - 52959-195-20 - (Sulindac)

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Drug Information of Sulindac

Product NDC: 52959-195
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: 52959-195
Labeler Name: H.J. Harkins Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071795
Marketing Category: ANDA
Start Marketing Date: 19900403

Package Information of Sulindac

Package NDC: 52959-195-20
Package Description: 20 TABLET in 1 BOTTLE, PLASTIC (52959-195-20)

NDC Information of Sulindac

NDC Code 52959-195-20
Proprietary Name Sulindac
Package Description 20 TABLET in 1 BOTTLE, PLASTIC (52959-195-20)
Product NDC 52959-195
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 H.J. Harkins Company, 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