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    NDC 00703-9514-03 Sulfamethoxazole and Trimethoprim 80; 16 mg/mL; mg/mL Details

    Sulfamethoxazole and Trimethoprim 80; 16 mg/mL; mg/mL

    Sulfamethoxazole and Trimethoprim is a INTRAVENOUS INJECTION, SOLUTION, CONCENTRATE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Teva Parenteral Medicines, Inc.. The primary component is SULFAMETHOXAZOLE; TRIMETHOPRIM.

    Product Information

    NDC 00703-9514
    Product ID 0703-9514_4f95c6e0-5888-4e8d-a0d6-3525dc2174c7
    Associated GPIs 16990002302010
    GCN Sequence Number 009393
    GCN Sequence Number Description sulfamethoxazole/trimethoprim VIAL 80-16MG/ML INTRAVEN
    HIC3 W2A
    HIC3 Description ABSORBABLE SULFONAMIDE ANTIBACTERIAL AGENTS
    GCN 90139
    HICL Sequence Number 004071
    HICL Sequence Number Description SULFAMETHOXAZOLE/TRIMETHOPRIM
    Brand/Generic Generic
    Proprietary Name Sulfamethoxazole and Trimethoprim
    Proprietary Name Suffix n/a
    Non-Proprietary Name Sulfamethoxazole and Trimethoprim
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form INJECTION, SOLUTION, CONCENTRATE
    Route INTRAVENOUS
    Active Ingredient Strength 80; 16
    Active Ingredient Units mg/mL; mg/mL
    Substance Name SULFAMETHOXAZOLE; TRIMETHOPRIM
    Labeler Name Teva Parenteral Medicines, Inc.
    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 ANDA073303
    Listing Certified Through 2024-12-31

    Package

    NDC 00703-9514-03 (00703951403)

    NDC Package Code 0703-9514-03
    Billing NDC 00703951403
    Package 10 VIAL, MULTI-DOSE in 1 CARTON (0703-9514-03) / 10 mL in 1 VIAL, MULTI-DOSE (0703-9514-01)
    Marketing Start Date 1991-11-01
    NDC Exclude Flag N
    Pricing Information N/A