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    NDC 63629-9863-01 Cevimeline Hydrochloride 30 mg/1 Details

    Cevimeline Hydrochloride 30 mg/1

    Cevimeline Hydrochloride is a ORAL CAPSULE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is CEVIMELINE HYDROCHLORIDE.

    Product Information

    NDC 63629-9863
    Product ID 63629-9863_671bdcca-bd56-4802-8b20-53eb0b01e789
    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 Cevimeline Hydrochloride
    Proprietary Name Suffix n/a
    Non-Proprietary Name Cevimeline Hydrochloride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form CAPSULE
    Route ORAL
    Active Ingredient Strength 30
    Active Ingredient Units mg/1
    Substance Name CEVIMELINE HYDROCHLORIDE
    Labeler Name Bryant Ranch Prepack
    Pharmaceutical Class Cholinergic Muscarinic Agonists [MoA], Cholinergic Receptor Agonist [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA203775
    Listing Certified Through 2024-12-31

    Package

    NDC 63629-9863-01 (63629986301)

    NDC Package Code 63629-9863-1
    Billing NDC 63629986301
    Package 30 CAPSULE in 1 BOTTLE (63629-9863-1)
    Marketing Start Date 2023-10-27
    NDC Exclude Flag N
    Pricing Information N/A