Search by Drug Name or NDC

    NDC 70934-0682-30 Dicyclomine Hydrochloride 20 mg/1 Details

    Dicyclomine Hydrochloride 20 mg/1

    Dicyclomine Hydrochloride is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Denton Pharma, Inc. DBA Northwind Pharmaceuticals. The primary component is DICYCLOMINE HYDROCHLORIDE.

    Product Information

    NDC 70934-0682
    Product ID 70934-682_f185706b-c2b4-61ac-e053-2995a90a982c
    Associated GPIs 49103010100305
    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 Dicyclomine Hydrochloride
    Proprietary Name Suffix n/a
    Non-Proprietary Name Dicyclomine Hydrochloride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 20
    Active Ingredient Units mg/1
    Substance Name DICYCLOMINE HYDROCHLORIDE
    Labeler Name Denton Pharma, Inc. DBA Northwind Pharmaceuticals
    Pharmaceutical Class Anticholinergic [EPC], Cholinergic Antagonists [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA085223
    Listing Certified Through n/a

    Package

    NDC 70934-0682-30 (70934068230)

    NDC Package Code 70934-682-30
    Billing NDC 70934068230
    Package 30 TABLET in 1 BOTTLE, PLASTIC (70934-682-30)
    Marketing Start Date 2020-04-29
    NDC Exclude Flag N
    Pricing Information N/A