Detrol LA - 55154-3935-0 - (tolterodine tartrate)

Alphabetical Index


Drug Information of Detrol LA

Product NDC: 55154-3935
Proprietary Name: Detrol LA
Non Proprietary Name: tolterodine tartrate
Active Ingredient(s): 2    mg/1 & nbsp;   tolterodine tartrate
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Detrol LA

Product NDC: 55154-3935
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021228
Marketing Category: NDA
Start Marketing Date: 20001222

Package Information of Detrol LA

Package NDC: 55154-3935-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-3935-0) > 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK

NDC Information of Detrol LA

NDC Code 55154-3935-0
Proprietary Name Detrol LA
Package Description 10 BLISTER PACK in 1 BAG (55154-3935-0) > 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC 55154-3935
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name tolterodine tartrate
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20001222
Marketing Category Name NDA
Labeler Name Cardinal Health
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 LA


General Information