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Drugs are identified and reported using a unique, three-segment number called the National Drug Code (NDC) which serves as the FDAs identifier for drugs. FDA publishes the listed NDC numbers in the NDC Directory which is updated daily.
New Drug Application (NDA) Number This six digit number is assigned by FDA staff to each application for approval to market a new drug in the United States. A drug can have more than one application number if it has different dosage forms or routes of administration.
The FDA Adverse Event Reporting System (FAERS) database contains information on adverse event and medication error reports submitted to FDA. The database is designed to support the FDAs post-marketing safety surveillance program for drug and therapeutic biologic products.
What is Erivedge? Erivedge (vismodegib) belongs to a class of medications called hedgehog pathway inhibitors. Vismodegib works by blocking the action of a protein that signals cancer cells to multiply. This helps stop or slow the spread of cancer cells and may help shrink tumors.
Vismodegib is a highly permeable compound with low aqueous solubility (BCS Class 2).
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The FDA has approved vismodegib (Erivedge) to treat adult patients with basal cell carcinoma, the most common type of skin cancer. The drug is intended for use in patients with locally advanced basal cell cancer who are not candidates for surgery or radiation and for patients with metastatic disease.
Vismodegib is a type of targeted therapy called a hedgehog pathway inhibitor. This means it works by targeting a pathway (series of signals or events) that drives cancer growth. Disrupting the Hedgehog signal prevents the cancer from growing.
Vismodegib is in a class of medications called hedgehog pathway inhibitors.

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