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NDC 00009-4541-02 Detrol 1 mg/1 Details

Detrol 1 mg/1

Detrol is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by PHARMACIA & UPJOHN COMPANY LLC. The primary component is TOLTERODINE TARTRATE.

MedlinePlus Drug Summary

Tolterodine is used treat overactive bladder (a condition in which the bladder muscles contract uncontrollably and cause frequent urination, urgent need to urinate, and inability to control urination). Tolterodine is in a class of medications called antimuscarinics. It works by relaxing the bladder muscles preventing bladder contraction.

Related Packages: 00009-4541-02
Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Tolterodine

Product Information

NDC	00009-4541
Product ID	0009-4541_bf08d786-0e54-423f-9e98-f7bbe89a27ab
Associated GPIs	54100060200320
GCN Sequence Number	039138
GCN Sequence Number Description	tolterodine tartrate TABLET 1 MG ORAL
HIC3	R1A
HIC3 Description	URINARY TRACT ANTISPASMODIC/ANTIINCONTINENCE AGENT
GCN	37061
HICL Sequence Number	018047
HICL Sequence Number Description	TOLTERODINE TARTRATE
Brand/Generic	Brand
Proprietary Name	Detrol
Proprietary Name Suffix	n/a
Non-Proprietary Name	tolterodine tartrate
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET, FILM COATED
Route	ORAL
Active Ingredient Strength	1
Active Ingredient Units	mg/1
Substance Name	TOLTERODINE TARTRATE
Labeler Name	PHARMACIA & UPJOHN COMPANY LLC
Pharmaceutical Class	Cholinergic Muscarinic Antagonist [EPC], Cholinergic Muscarinic Antagonists [MoA]
DEA Schedule	n/a
Marketing Category	NDA
Application Number	NDA020771
Listing Certified Through	2024-12-31

Package

NDC 00009-4541-02 (00009454102)

Pricing Information	N/A
NDC Package Code	0009-4541-02
Billing NDC	00009454102
Package	60 TABLET, FILM COATED in 1 BOTTLE (0009-4541-02)
Marketing Start Date	1998-03-25
NDC Exclude Flag	N