Detrol LA
These highlights do not include all the information needed to use Detrol LA safely and effectively. See full prescribing information for Detrol LA. Detrol LA (tolterodine tartrate extended release capsules)For oral administrationInitial U.S. Approval: December 2000
Approved
Approval ID
88df13b1-090d-4894-a60a-878b370409c0
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Mar 23, 2017
Manufacturers
FDA
Avera McKennan Hospital
DUNS: 068647668
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
tolterodine tartrate
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code69189-5190
Application NumberNDA021228
Product Classification
M
Marketing Category
C73594
G
Generic Name
tolterodine tartrate
Product Specifications
Route of AdministrationORAL
Effective DateMarch 23, 2017
FDA Product Classification
INGREDIENTS (9)
TOLTERODINE TARTRATEActive
Quantity: 2 mg in 1 1
Code: 5T619TQR3R
Classification: ACTIB
ETHYLCELLULOSESInactive
Code: 7Z8S9VYZ4B
Classification: IACT
SUCROSEInactive
Code: C151H8M554
Classification: IACT
HYPROMELLOSESInactive
Code: 3NXW29V3WO
Classification: IACT
MEDIUM-CHAIN TRIGLYCERIDESInactive
Code: C9H2L21V7U
Classification: IACT
OLEIC ACIDInactive
Code: 2UMI9U37CP
Classification: IACT
GELATINInactive
Code: 2G86QN327L
Classification: IACT
FD&C BLUE NO. 2Inactive
Code: L06K8R7DQK
Classification: IACT
FERRIC OXIDE YELLOWInactive
Code: EX438O2MRT
Classification: IACT