Detrol - 0009-4544-03 - (tolterodine tartrate)

Alphabetical Index


Drug Information of Detrol

Product NDC: 0009-4544
Proprietary Name: Detrol
Non Proprietary Name: tolterodine tartrate
Active Ingredient(s): 2    mg/1 & nbsp;   tolterodine tartrate
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Detrol

Product NDC: 0009-4544
Labeler Name: Pharmacia and Upjohn Company
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020771
Marketing Category: NDA
Start Marketing Date: 19980325

Package Information of Detrol

Package NDC: 0009-4544-03
Package Description: 500 TABLET, FILM COATED in 1 BOTTLE (0009-4544-03)

NDC Information of Detrol

NDC Code 0009-4544-03
Proprietary Name Detrol
Package Description 500 TABLET, FILM COATED in 1 BOTTLE (0009-4544-03)
Product NDC 0009-4544
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name tolterodine tartrate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19980325
Marketing Category Name NDA
Labeler Name Pharmacia and Upjohn Company
Substance Name TOLTERODINE TARTRATE
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA]

Complete Information of Detrol


General Information