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    NDC 58809-0555-08 VANACOF DM 18; 200; 10 mg/15mL; mg/15mL; mg/15mL Details

    VANACOF DM 18; 200; 10 mg/15mL; mg/15mL; mg/15mL

    VANACOF DM is a ORAL LIQUID in the HUMAN OTC DRUG category. It is labeled and distributed by GM Pharmaceuticals, INC. The primary component is DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE.

    Product Information

    NDC 58809-0555
    Product ID 58809-555_02abdf72-4dde-715e-e063-6394a90a91e7
    Associated GPIs 43997303100965
    GCN Sequence Number 071093
    GCN Sequence Number Description guaifen/dextromethorphan/PE LIQUID 18-10MG/15 ORAL
    HIC3 B4R
    HIC3 Description NON-OPIOID ANTITUSSIVE-DECONGESTANT-EXPECTORANT
    GCN 34782
    HICL Sequence Number 000216
    HICL Sequence Number Description GUAIFENESIN/DEXTROMETHORPHAN HBR/PHENYLEPHRINE
    Brand/Generic Brand
    Proprietary Name VANACOF DM
    Proprietary Name Suffix n/a
    Non-Proprietary Name DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE
    Product Type HUMAN OTC DRUG
    Dosage Form LIQUID
    Route ORAL
    Active Ingredient Strength 18; 200; 10
    Active Ingredient Units mg/15mL; mg/15mL; mg/15mL
    Substance Name DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
    Labeler Name GM Pharmaceuticals, INC
    Pharmaceutical Class Adrenergic alpha1-Agonists [MoA], Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE], Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC
    DEA Schedule n/a
    Marketing Category OTC MONOGRAPH FINAL
    Application Number part341
    Listing Certified Through 2024-12-31

    Package

    NDC 58809-0555-08 (58809055508)

    NDC Package Code 58809-555-08
    Billing NDC 58809055508
    Package 240 mL in 1 BOTTLE (58809-555-08)
    Marketing Start Date 2013-06-01
    NDC Exclude Flag N
    Pricing Information N/A