Drugs Supplement Type Code and Description

$79 / year

This dataset contains the Document Type Lookup part to build the Drugs@FDA database. Drugs at FDA is a database of FDA Approved Drug Products available in the FDA official website for search by drug name, active ingredient or application number. It provides information of drug (generic) name, active ingredient, form and strength available, FDA application number, label info, dosage form or route, marketing status and pharmaceutical company as well as patient information, approval letters, review and other facts for drugs approved after 1997. The information is classified by health information, regulatory information and advanced search. This dataset contains the necessary technical information (excluding programming scripts) to reproduce the online version of Drugs@FDA.

Complexity

Drugs at FDA allows to search for official information about FDA (Food and Drug Administration) approved innovator and generic drugs and therapeutic biological products. The main uses of Drugs@FDA are: finding labels for approved drug products, generic drug products for an innovator drug product, therapeutically equivalent drug products for an innovator or generic drug product, consumer information for drugs approved from 1998 on, all drugs with a specific active ingredient, viewing the approval history of a drug.

Drugs@FDA contains prescription and over-the-counter human drugs and therapeutic biologicals currently approved for sale in the United States. Drugs@FDA includes discontinued drugs and “Chemical Type 6″ approvals.

Drugs@FDA contains the following therapeutic biological products:
– monoclonal antibodies
– cytokines, growth factors, enzymes, immunomodulators; and thrombolytics
– proteins intended for therapeutic use that are extracted from animals or microorganisms, including recombinant versions of these products (except clotting factors)
– other non-vaccine therapeutic immunotherapies

Not all therapeutic biological products are in Drugs@FDA.
Drugs@FDA contains most of the drug products approved since 1939. The majority of labels, approval letters, reviews, and other information are available for drug products approved from 1998 to the present.

Drugs@FDA does not include:
– over-the-counter (OTC) products approved for marketing through a process other than submission of a New Drug Application or Biologic License Application
– drugs sold outside the United States that are not approved for marketing in the U.S.
– drugs not approved by the FDA
– drugs under review at FDA for which no action (approved or not approved) has occurred yet
– dietary supplements, which do not require FDA approval to be sold in the United States
– biological products regulated by the Center for Biologics Evaluation and Research
– animal drugs, which are regulated by the Center for Veterinary Medicine”

Document Type Lookup refers to supplement type code and description to the application number.

Source: US Food and Drug Administration, F.D.A. (2016). FDA.gov. Retrieved 8 May, 2016.

Date Created

2016

Last Modified

2016-07-13

Version

2016-07-02

Update Frequency

Weekly

Temporal Coverage

2016

Spatial Coverage

N/A

Source

John Snow Labs => US Food and Drug Administration

Source License URL

John Snow Labs Standard License

Source License Requirements

N/A

Source Citation

N/A

Keywords

Drugs Database, SQL Database, SQL Drugs Database, Online Drug Database, FDA Approved Drug Products, Drugs FDA, FDA Official Drug Website, FDA Generic Drugs List, FDA Therapeutic Biological Products

Other Titles

Drugs at FDA Database Products, Drugs at FDA Document Type Lookup, FDA Document Type Lookup

NameDescriptionTypeConstraints
Supplement_Type_CodeA supplement is an application to allow a company to make changes in a product that already has an approved new drug application (NDA). The supplement type refers to the kind of change that was approved by FDA. This includes changes in manufacturing, patient population, and formulation.string-
Supplement_Type_DescriptionDescription of supplement type code of the application numberstring-
Supplement_Type_CodeSupplement_Type_Description
SDC
SEF
SBSBA
SOOther
NApproval
SLLabeling
SSupplement
SCChemistry
MPresubmission
SDSDistributor