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    NDC 80725-0250-01 Humatin 250 mg/1 Details

    Humatin 250 mg/1

    Humatin is a ORAL CAPSULE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Waylis Therapeutics LLC. The primary component is PAROMOMYCIN SULFATE.

    Product Information

    NDC 80725-0250
    Product ID 80725-250_218563ce-a4f4-490b-99fe-eabc713bbdba
    Associated GPIs 07000055100110
    GCN Sequence Number 009585
    GCN Sequence Number Description paromomycin sulfate CAPSULE 250 MG ORAL
    HIC3 W4C
    HIC3 Description AMEBICIDES
    GCN 42970
    HICL Sequence Number 004155
    HICL Sequence Number Description PAROMOMYCIN SULFATE
    Brand/Generic Brand
    Proprietary Name Humatin
    Proprietary Name Suffix n/a
    Non-Proprietary Name PAROMOMYCIN SULFATE
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form CAPSULE
    Route ORAL
    Active Ingredient Strength 250
    Active Ingredient Units mg/1
    Substance Name PAROMOMYCIN SULFATE
    Labeler Name Waylis Therapeutics LLC
    Pharmaceutical Class Antiprotozoal [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA065173
    Listing Certified Through 2024-12-31

    Package

    NDC 80725-0250-01 (80725025001)

    NDC Package Code 80725-250-01
    Billing NDC 80725025001
    Package 100 CAPSULE in 1 BOTTLE (80725-250-01)
    Marketing Start Date 2021-04-08
    NDC Exclude Flag N
    Pricing Information N/A