Sulindac - 0378-0427-01 - (sulindac)

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Drug Information of Sulindac

Product NDC: 0378-0427
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: 0378-0427
Labeler Name: Mylan Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA073039
Marketing Category: ANDA
Start Marketing Date: 20120802

Package Information of Sulindac

Package NDC: 0378-0427-01
Package Description: 100 TABLET in 1 BOTTLE, PLASTIC (0378-0427-01)

NDC Information of Sulindac

NDC Code 0378-0427-01
Proprietary Name Sulindac
Package Description 100 TABLET in 1 BOTTLE, PLASTIC (0378-0427-01)
Product NDC 0378-0427
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name sulindac
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120802
Marketing Category Name ANDA
Labeler Name Mylan Pharmaceuticals Inc.
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