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    NDC 68788-7835-02 ACETAMINOPHEN AND CODEINE PHOSPHATE 300; 30 mg/1; mg/1 Details

    ACETAMINOPHEN AND CODEINE PHOSPHATE 300; 30 mg/1; mg/1

    ACETAMINOPHEN AND CODEINE PHOSPHATE is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Preferred Pharmaceuticals Inc.. The primary component is ACETAMINOPHEN; CODEINE PHOSPHATE.

    Product Information

    NDC 68788-7835
    Product ID 68788-7835_f33f3617-375c-4d2b-80f7-119265552514
    Associated GPIs 65991002050315
    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 ACETAMINOPHEN AND CODEINE PHOSPHATE
    Proprietary Name Suffix n/a
    Non-Proprietary Name acetaminophen and codeine phosphate
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 300; 30
    Active Ingredient Units mg/1; mg/1
    Substance Name ACETAMINOPHEN; CODEINE PHOSPHATE
    Labeler Name Preferred Pharmaceuticals Inc.
    Pharmaceutical Class Full Opioid Agonists [MoA], Opioid Agonist [EPC]
    DEA Schedule CIII
    Marketing Category ANDA
    Application Number ANDA040419
    Listing Certified Through 2024-12-31

    Package

    NDC 68788-7835-02 (68788783502)

    NDC Package Code 68788-7835-2
    Billing NDC 68788783502
    Package 20 TABLET in 1 BOTTLE (68788-7835-2)
    Marketing Start Date 2021-01-18
    NDC Exclude Flag N
    Pricing Information N/A