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    NDC 12539-0144-01 Uretron D/S .12; 81.6; 10.8; 36.2; 40.8 mg/1; mg/1; mg/1; mg/1; mg/1 Details

    Uretron D/S .12; 81.6; 10.8; 36.2; 40.8 mg/1; mg/1; mg/1; mg/1; mg/1

    Uretron D/S is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by A.G. Marin Pharmaceutical. The primary component is HYOSCYAMINE SULFATE; METHENAMINE; METHYLENE BLUE; PHENYL SALICYLATE; SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE.

    Product Information

    NDC 12539-0144
    Product ID 12539-144_ea74f1aa-2b4e-4ccf-e053-2995a90abab5
    Associated GPIs 16992005200322
    GCN Sequence Number 062986
    GCN Sequence Number Description meth/meblue/sod phos/psal/hyos TABLET 81.6-10.8 ORAL
    HIC3 W2G
    HIC3 Description ANTIBIOTIC, ANTIBACTERIAL, MISC.
    GCN 98746
    HICL Sequence Number 034934
    HICL Sequence Number Description METHENAMINE/METHYLENE BLUE/SOD PHOS/P.SALICYLATE/HYOSCYAMINE
    Brand/Generic Brand
    Proprietary Name Uretron D/S
    Proprietary Name Suffix n/a
    Non-Proprietary Name Methenamine, Sodium Phosphate Monobasic, Phenyl Salicylate, Methylene Blue, and Hyoscyamine Sulfate
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength .12; 81.6; 10.8; 36.2; 40.8
    Active Ingredient Units mg/1; mg/1; mg/1; mg/1; mg/1
    Substance Name HYOSCYAMINE SULFATE; METHENAMINE; METHYLENE BLUE; PHENYL SALICYLATE; SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE
    Labeler Name A.G. Marin Pharmaceutical
    Pharmaceutical Class Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC], Oxidation-Reduction Activity [MoA], Oxidation-Reduction Agent [EPC]
    DEA Schedule n/a
    Marketing Category UNAPPROVED DRUG OTHER
    Application Number n/a
    Listing Certified Through 2023-12-31

    Package

    NDC 12539-0144-01 (12539014401)

    NDC Package Code 12539-144-01
    Billing NDC 12539014401
    Package 100 TABLET in 1 BOTTLE (12539-144-01)
    Marketing Start Date 2022-10-07
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL ea74f1aa-2b4d-4ccf-e053-2995a90abab5 Details

    Revised: 10/2022