The FDA DMF List contains Drug Master Files recieved by the FDA. This file is updated by the FDA quarterly. For reference "A" = Active, "I" = Inactive and DMF types include. Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable) Type II Drug Substance, Drug Substance Intermediate, and Material Used in Their Preparation, or Drug Product Type III Packaging Material Type IV Excipient, Colorant, Flavor, Essence, or Material Used in Their Preparation Type V FDA Accepted Reference Information
The manufacturing site inspection classification file list the status classification of sites registered with the FDA. The classifications include NAI "No Action Indicated", VAI "Voluntary Action Indicated" or OAI "Official Action Indicated". This includes classifications from 10.1.2008 to 9.30.2016
This is an excel download of a portion of the FDA Orange book which contains the status of Approved Drugs with Therapeutic Equivelance Evaluations. The FDA updates this data set monthly and was built with data downloaded June 10th 2017
This is a easily searchable online database of a portion of the FDA Orange book which contains the status of Approved Drugs with Therapeutic Equivelance Evaluations.
This is a link to the FDA Orange book which contains the status of Approved Drugs with Therapeutic Equivelance Evaluations.
This database can be searched to see the details of US drugs including product cartons and labels.
This link will take you to ClinicalTrials.gov which is a United States Government Database of clinical trials. At this site you can search clinical trials across various stages of completion and by indication.
This link will take you to a list of the drug spend for Medicaid
This link will take you to a list of the drug spend for Medicare