POST api/ListDESIStatuses

Returns the FDA-assigned DESI statuses, along with their internal identifiers. Includes a ‘MaxResults’ option that allows you to limit the number of results returned.

Prior to 1962, drug marketers in the US were not required to submit efficacy studies to the FDA for a drug approval. As part of the Drug Efficacy and Safety Implementation (DESI), all drug products submissions are required. Products marketed pre-1962 are required to have efficacy data submitted for evaluation. The FDA assigns a DESI code to each of these products.

API Method Test Client

Request Information

URI Parameters

None.

Body Parameters

ListDESIStatusesRequest

Name	Description	Type	Additional information
MaxResults	Limits the number of results returned. A null value means no limit, and everthing will be returned.	integer	None.
AccessToken	Temporary access token from the GSDD Auth API. Used to validate your license. Note: Access tokens are temporary and may be invalidated early for various reasons, including—but not limited to—site maintenance and security updates. If a token is invalidated prematurely, simply request new tokens via the AccessToken method in the GSDD Auth API. This is a rather rare occurrence, but should be planned for and handled by the consuming application.	string	Required

Request Formats

application/json, text/json

Sample:

{
  "MaxResults": 10,
  "AccessToken": "T25lX0hhcHB5X0FuZF9TYXRpc2ZpZWRfR1NERF9DdXN0b21lcl9TYW1wbGVfQWNjZXNzVG9rZW4="
}

Response Information

Resource Description

ListDESIStatusesResponse

Name	Description	Type	Additional information
DESIStatuses	Returns the output parameters for the FDA-assigned DESI statuses.	Collection of IdentifierName	None.

Response Formats

application/json, text/json

Sample:

{
  "DESIStatuses": [
    {
      "Id": 1,
      "Name": "Sample Name text."
    },
    {
      "Id": 2,
      "Name": "Sample Name text."
    }
  ]
}