Detrol LA - 0009-5190-01 - (tolterodine tartrate)

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Drug Information of Detrol LA

Product NDC: 0009-5190
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: 0009-5190
Labeler Name: Pharmacia and Upjohn Company
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021228
Marketing Category: NDA
Start Marketing Date: 20000222

Package Information of Detrol LA

Package NDC: 0009-5190-01
Package Description: 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0009-5190-01)

NDC Information of Detrol LA

NDC Code 0009-5190-01
Proprietary Name Detrol LA
Package Description 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0009-5190-01)
Product NDC 0009-5190
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name tolterodine tartrate
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20000222
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 LA


General Information