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    NDC 76420-0619-20 Ivermectin 3 mg/1 Details

    Ivermectin 3 mg/1

    Ivermectin is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Asclemed USA, Inc.. The primary component is IVERMECTIN.

    Product Information

    NDC 76420-0619
    Product ID 76420-619_06f2293c-2cf4-70d4-e063-6394a90a3a56
    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 Ivermectin
    Proprietary Name Suffix n/a
    Non-Proprietary Name Ivermectin
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 3
    Active Ingredient Units mg/1
    Substance Name IVERMECTIN
    Labeler Name Asclemed USA, Inc.
    Pharmaceutical Class Antiparasitic [EPC], Pediculicide [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA204154
    Listing Certified Through 2024-12-31

    Package

    NDC 76420-0619-20 (76420061920)

    NDC Package Code 76420-619-20
    Billing NDC 76420061920
    Package 2 BLISTER PACK in 1 CARTON (76420-619-20) / 10 TABLET in 1 BLISTER PACK
    Marketing Start Date 2023-10-05
    NDC Exclude Flag N
    Pricing Information N/A