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    NDC 68788-7844-01 Cefdinir 250 mg/5mL Details

    Cefdinir 250 mg/5mL

    Cefdinir is a ORAL POWDER, FOR SUSPENSION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Preferred Pharmaceuticals Inc.. The primary component is CEFDINIR.

    Product Information

    NDC 68788-7844
    Product ID 68788-7844_1cb342e5-93b4-4627-8a3f-ca77622afd3d
    Associated GPIs 02300040001930
    GCN Sequence Number n/a
    GCN Sequence Number Description n/a
    HIC3 n/a
    HIC3 Description n/a
    GCN n/a
    HICL Sequence Number n/a
    HICL Sequence Number Description n/a
    Brand/Generic n/a
    Proprietary Name Cefdinir
    Proprietary Name Suffix n/a
    Non-Proprietary Name Cefdinir
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form POWDER, FOR SUSPENSION
    Route ORAL
    Active Ingredient Strength 250
    Active Ingredient Units mg/5mL
    Substance Name CEFDINIR
    Labeler Name Preferred Pharmaceuticals Inc.
    Pharmaceutical Class Cephalosporin Antibacterial [EPC], Cephalosporins [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA065473
    Listing Certified Through 2024-12-31

    Package

    NDC 68788-7844-01 (68788784401)

    NDC Package Code 68788-7844-1
    Billing NDC 68788784401
    Package 1 BOTTLE in 1 CARTON (68788-7844-1) / 100 mL in 1 BOTTLE
    Marketing Start Date 2021-01-20
    NDC Exclude Flag N
    Pricing Information N/A