Lialda - 54092-476-01 - (mesalamine)

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Drug Information of Lialda

Product NDC: 54092-476
Proprietary Name: Lialda
Non Proprietary Name: mesalamine
Active Ingredient(s): 1.2    g/1 & nbsp;   mesalamine
Administration Route(s): ORAL
Dosage Form(s): TABLET, DELAYED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Lialda

Product NDC: 54092-476
Labeler Name: Shire US Manufacturing Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022000
Marketing Category: NDA
Start Marketing Date: 20070116

Package Information of Lialda

Package NDC: 54092-476-01
Package Description: 120 TABLET, DELAYED RELEASE in 1 BOTTLE (54092-476-01)

NDC Information of Lialda

NDC Code 54092-476-01
Proprietary Name Lialda
Package Description 120 TABLET, DELAYED RELEASE in 1 BOTTLE (54092-476-01)
Product NDC 54092-476
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name mesalamine
Dosage Form Name TABLET, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20070116
Marketing Category Name NDA
Labeler Name Shire US Manufacturing Inc.
Substance Name MESALAMINE
Strength Number 1.2
Strength Unit g/1
Pharmaceutical Classes Aminosalicylate [EPC],Aminosalicylic Acids [Chemical/Ingredient]

Complete Information of Lialda


General Information