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NDC 00009-4544-02 Detrol 2 mg/1 Details
Detrol 2 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: 00009-4544-02Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Tolterodine
Product Information
NDC | 00009-4544 |
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Product ID | 0009-4544_bf08d786-0e54-423f-9e98-f7bbe89a27ab |
Associated GPIs | 54100060200330 |
GCN Sequence Number | 039139 |
GCN Sequence Number Description | tolterodine tartrate TABLET 2 MG ORAL |
HIC3 | R1A |
HIC3 Description | URINARY TRACT ANTISPASMODIC/ANTIINCONTINENCE AGENT |
GCN | 37062 |
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 | 2 |
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 00009-4544-02 (00009454402)
NDC Package Code | 0009-4544-02 |
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Billing NDC | 00009454402 |
Package | 60 TABLET, FILM COATED in 1 BOTTLE (0009-4544-02) |
Marketing Start Date | 1998-03-25 |
NDC Exclude Flag | N |
Pricing Information | N/A |