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    NDC 71863-0110-50 Alkindi 1 mg/1 Details

    Alkindi 1 mg/1

    Alkindi is a ORAL GRANULE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Eton Pharmaceuticals, Inc.. The primary component is HYDROCORTISONE.

    Product Information

    NDC 71863-0110
    Product ID 71863-110_08f49aef-a4f1-da40-e063-6294a90ab218
    Associated GPIs 22100025006815
    GCN Sequence Number 079920
    GCN Sequence Number Description hydrocortisone CAP SPRINK 1 MG ORAL
    HIC3 P5A
    HIC3 Description GLUCOCORTICOIDS
    GCN 46548
    HICL Sequence Number 002867
    HICL Sequence Number Description HYDROCORTISONE
    Brand/Generic Brand
    Proprietary Name Alkindi
    Proprietary Name Suffix Sprinkle
    Non-Proprietary Name Hydrocortisone
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form GRANULE
    Route ORAL
    Active Ingredient Strength 1
    Active Ingredient Units mg/1
    Substance Name HYDROCORTISONE
    Labeler Name Eton Pharmaceuticals, Inc.
    Pharmaceutical Class Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
    DEA Schedule n/a
    Marketing Category NDA
    Application Number NDA213876
    Listing Certified Through 2024-12-31

    Package

    NDC 71863-0110-50 (71863011050)

    NDC Package Code 71863-110-50
    Billing NDC 71863011050
    Package 1 BOTTLE, PLASTIC in 1 CARTON (71863-110-50) / 50 GRANULE in 1 BOTTLE, PLASTIC
    Marketing Start Date 2020-09-29
    NDC Exclude Flag N
    Pricing Information N/A