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87 datasets found for "organization:hhs-gov AND type:dataset"
  • Federal

    National Drug Code Directory 94 recent views

    U.S. Department of Health & Human Services —

    The Drug Listing Act of 1972 requires registered drug establishments to provide the Food and Drug Administration (FDA) with a current list of all drugs manufactured,...
  • Federal

    Drugs@FDA Database 28 recent views

    U.S. Department of Health & Human Services —

    Information about FDA-approved brand name and generic prescription and over-the-counter human drugs and biological therapeutic products. Drugs@FDA includes most of...
  • Federal

    Inactive ingredient Search for Approved Drug Products 17 recent views

    U.S. Department of Health & Human Services —

    According to 21 CFR 210.3(b)(8), an inactive ingredient is any component of a drug product other than the active ingredient. Only inactive ingredients in the final...
  • Federal

    CLIA Currently Waived Analytes 15 recent views

    U.S. Department of Health & Human Services —

    This database contains the commercially marketed in vitro test systems categorized as CLIA waived by the FDA since January 31, 2000, and by the Centers for Disease...
  • Federal

    Drug Establishments Current Registration Site 15 recent views

    U.S. Department of Health & Human Services —

    The Drug Establishments Current Registration Site (DECRS) is a database of current information submitted by drug firms to register establishments (facilities) which...
  • Federal

    Adverse Event Reporting System (AERS) 14 recent views

    U.S. Department of Health & Human Services —

    The Adverse Event Reporting System (AERS) is a computerized information database designed to support the FDA's post-marketing safety surveillance program for all...
  • Federal

    FDA Adverse Event Reporting System (FAERS): Latest Quartely Data Files 14 recent views

    U.S. Department of Health & Human Services —

    The FDA Adverse Event Reporting System (FAERS) is a database that contains information on adverse event and medication error reports submitted to FDA. The database is...
  • Federal

    NHRIC (National Health Related Items Code) 11 recent views

    U.S. Department of Health & Human Services —

    The National Health Related Items Code (NHRIC) is a system for identification and numbering of marketed device packages that is compatible with other numbering...
  • Federal

    Approved Animal Drug Products (Green Book) 10 recent views

    U.S. Department of Health & Human Services —

    On November 16, 1988, the President of the United States signed into law the Generic Animal Drug and Patent Restoration Act (GADPTRA). Among its major provisions, the...
  • Federal

    Total Product Life Cycle (TPLC) 10 recent views

    U.S. Department of Health & Human Services —

    The Total Product Life Cycle (TPLC) database integrates premarket and postmarket data about medical devices. It includes information pulled from CDRH databases...
  • Federal

    Orange Book

    U.S. Department of Health & Human Services —

    The Approved Drug Products with Therapeutic Equivalence (Orange Book or OB) is a list of drugs approved under Section 505 of the Federal Food, Drug and Cosmetic Act...
  • Federal

    Product Classification

    U.S. Department of Health & Human Services —

    This database contains medical device names and associated information developed by the Center. It includes a three letter device product code and a Device Class that...
  • Federal

    Dissolution Methods Database

    U.S. Department of Health & Human Services —

    For a drug product that does not have a dissolution test method in the United States Pharmacopeia (USP), the FDA Dissolution Methods Database provides information on...
  • Federal

    FDA Recognized Consensus Standards

    U.S. Department of Health & Human Services —

    This database consists of those national and international standards recognized by FDA which manufacturers can declare conformity to and is part of the information...
  • Federal

    FDA Abbott Infant Formula Recall

    U.S. Department of Health & Human Services —

    On September 22, 2010, Abbott issued a voluntary recall of certain Similac powdered infant formula after identifying a common warehouse beetle (both larvae and...
  • Federal

    Inspection Database

    U.S. Department of Health & Human Services —

    FDA is disclosing the final inspection classification for inspections related to currently marketed FDA-regulated products. The disclosure of this information is not...
  • Federal

    Current and Resolved Drug Shortages and Discontinuations Reported to FDA

    U.S. Department of Health & Human Services —

    Information provided to FDA by manufacturers about current drugs in shortage, resolved shortages, and discontinuations of specific drug products.
  • Federal

    FDA Drug Label Data

    U.S. Department of Health & Human Services —

    This file contains the data elements used for searching the FDA Online Data Repository including proprietary name, active ingredients, marketing application number or...
  • Federal

    MedWatch Safety Alerts for Human Medical Products

    U.S. Department of Health & Human Services —

    MedWatch alerts provide timely new safety information on human drugs, medical devices, vaccines and other biologics, dietary supplements, and cosmetics. The alerts...
  • Federal

    Blood Establishment Registration Database

    U.S. Department of Health & Human Services —

    This application provides information for active, inactive, and pre-registered firms. Query options are by FEI, Applicant Name, Establishment Name, Other Names,...
87 datasets found for "organization:hhs-gov AND type:dataset"

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