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    NDC 61919-0645-10 Sulfameth/Trimeth-DS 800; 160 mg/1; mg/1 Details

    Sulfameth/Trimeth-DS 800; 160 mg/1; mg/1

    Sulfameth/Trimeth-DS is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Direct_Rx. The primary component is SULFAMETHOXAZOLE; TRIMETHOPRIM.

    Product Information

    NDC 61919-0645
    Product ID 61919-645_fb5919ec-f2fe-2123-e053-6394a90a1882
    Associated GPIs 16990002300320
    GCN Sequence Number 009396
    GCN Sequence Number Description sulfamethoxazole/trimethoprim TABLET 800-160 MG ORAL
    HIC3 W2A
    HIC3 Description ABSORBABLE SULFONAMIDE ANTIBACTERIAL AGENTS
    GCN 90163
    HICL Sequence Number 004071
    HICL Sequence Number Description SULFAMETHOXAZOLE/TRIMETHOPRIM
    Brand/Generic Generic
    Proprietary Name Sulfameth/Trimeth-DS
    Proprietary Name Suffix n/a
    Non-Proprietary Name Sulfameth/Trimeth-DS
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 800; 160
    Active Ingredient Units mg/1; mg/1
    Substance Name SULFAMETHOXAZOLE; TRIMETHOPRIM
    Labeler Name Direct_Rx
    Pharmaceutical Class Cytochrome P450 2C8 Inhibitors [MoA], Cytochrome P450 2C9 Inhibitors [MoA], Dihydrofolate Reductase Inhibitor Antibacterial [EPC], Dihydrofolate Reductase Inhibitors [MoA], Organic Cation Transporter 2 Inhibitors [MoA], Sulfonamide Antimicrobial [EPC], Su
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA090624
    Listing Certified Through 2024-12-31

    Package

    NDC 61919-0645-10 (61919064510)

    NDC Package Code 61919-645-10
    Billing NDC 61919064510
    Package 10 TABLET in 1 BOTTLE (61919-645-10)
    Marketing Start Date 2019-07-17
    NDC Exclude Flag N
    Pricing Information N/A