Glyset - 0009-5012-01 - (MIGLITOL)

Alphabetical Index


Drug Information of Glyset

Product NDC: 0009-5012
Proprietary Name: Glyset
Non Proprietary Name: MIGLITOL
Active Ingredient(s): 25    mg/1 & nbsp;   MIGLITOL
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Glyset

Product NDC: 0009-5012
Labeler Name: Pharmacia and Upjohn Company
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020682
Marketing Category: NDA
Start Marketing Date: 19961218

Package Information of Glyset

Package NDC: 0009-5012-01
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE (0009-5012-01)

NDC Information of Glyset

NDC Code 0009-5012-01
Proprietary Name Glyset
Package Description 100 TABLET, FILM COATED in 1 BOTTLE (0009-5012-01)
Product NDC 0009-5012
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name MIGLITOL
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19961218
Marketing Category Name NDA
Labeler Name Pharmacia and Upjohn Company
Substance Name MIGLITOL
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes alpha Glucosidase Inhibitors [MoA],alpha-Glucosidase Inhibitor [EPC]

Complete Information of Glyset


General Information