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    NDC 71205-0319-90 Tolterodine Tartrate 1 mg/1 Details

    Tolterodine Tartrate 1 mg/1

    Tolterodine Tartrate is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Proficient Rx LP. The primary component is TOLTERODINE TARTRATE.

    Product Information

    NDC 71205-0319
    Product ID 71205-319_df5371c1-a1d3-4e6d-af7a-17cb46d7653d
    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 Generic
    Proprietary Name Tolterodine Tartrate
    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 Proficient Rx LP
    Pharmaceutical Class Cholinergic Muscarinic Antagonist [EPC], Cholinergic Muscarinic Antagonists [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA077006
    Listing Certified Through 2024-12-31

    Package

    NDC 71205-0319-90 (71205031990)

    NDC Package Code 71205-319-90
    Billing NDC 71205031990
    Package 90 TABLET, FILM COATED in 1 BOTTLE (71205-319-90)
    Marketing Start Date 2019-09-01
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL b77f9893-a422-423a-bb27-527377ade36d Details

    Revised: 10/2019