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    NDC 68788-8115-06 cefdinir 125 mg/5mL Details

    cefdinir 125 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 68788-8115
    Product ID 68788-8115_58fabf70-c5a2-482c-8352-897d476a239e
    Associated GPIs
    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 125
    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 ANDA210534
    Listing Certified Through 2024-12-31

    Package

    NDC 68788-8115-06 (68788811506)

    NDC Package Code 68788-8115-6
    Billing NDC 68788811506
    Package 60 mL in 1 BOTTLE (68788-8115-6)
    Marketing Start Date 2021-12-07
    NDC Exclude Flag N
    Pricing Information N/A