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New Drug Application (NDA): 017481
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
VERMOX MEBENDAZOLE 100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** TABLET, CHEWABLE;ORAL Discontinued None Yes No
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels,
Patient Package Insert
Note Url
06/13/2017 SUPPL-47 Labeling-Package Insert Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2017/017481s047lbl.pdf
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