Asacol - 0149-0752-17 - (mesalamine)

Alphabetical Index


Drug Information of Asacol

Product NDC: 0149-0752
Proprietary Name: Asacol
Non Proprietary Name: mesalamine
Active Ingredient(s): 400    mg/1 & nbsp;   mesalamine
Administration Route(s): ORAL
Dosage Form(s): TABLET, DELAYED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Asacol

Product NDC: 0149-0752
Labeler Name: Procter & Gamble Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019651
Marketing Category: NDA
Start Marketing Date: 19920401

Package Information of Asacol

Package NDC: 0149-0752-17
Package Description: 1 BOTTLE in 1 CARTON (0149-0752-17) > 12 TABLET, DELAYED RELEASE in 1 BOTTLE

NDC Information of Asacol

NDC Code 0149-0752-17
Proprietary Name Asacol
Package Description 1 BOTTLE in 1 CARTON (0149-0752-17) > 12 TABLET, DELAYED RELEASE in 1 BOTTLE
Product NDC 0149-0752
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name mesalamine
Dosage Form Name TABLET, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 19920401
Marketing Category Name NDA
Labeler Name Procter & Gamble Pharmaceuticals, Inc.
Substance Name MESALAMINE
Strength Number 400
Strength Unit mg/1
Pharmaceutical Classes Aminosalicylate [EPC],Aminosalicylic Acids [Chemical/Ingredient]

Complete Information of Asacol


General Information