Detrol LA - 35356-417-30 - (tolterodine tartrate)

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Drug Information of Detrol LA

Product NDC: 35356-417
Proprietary Name: Detrol LA
Non Proprietary Name: tolterodine tartrate
Active Ingredient(s): 4    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: 35356-417
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021228
Marketing Category: NDA
Start Marketing Date: 20120228

Package Information of Detrol LA

Package NDC: 35356-417-30
Package Description: 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (35356-417-30)

NDC Information of Detrol LA

NDC Code 35356-417-30
Proprietary Name Detrol LA
Package Description 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (35356-417-30)
Product NDC 35356-417
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name tolterodine tartrate
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20120228
Marketing Category Name NDA
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Substance Name TOLTERODINE TARTRATE
Strength Number 4
Strength Unit mg/1
Pharmaceutical Classes Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA]

Complete Information of Detrol LA


General Information