86 datasets found for "organization:((hhs-gov) OR (nlm-nih-gov) OR (cdc-hhs-gov) OR (acf-hhs-gov) OR (ahrq-hhs-gov) OR (cms-hhs-gov) OR (npdb-hrsa-gov) OR (aoa-hhs-gov) OR (hrsa-gov) OR (samhsa-hhs-gov) OR (fda-hhs-gov) OR (ihs-hhs-gov) OR (nih-hhs-gov))"
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Federal
National Drug Code Directory 113 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
Drug Establishments Current Registration Site 33 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
Drugs@FDA Database 31 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
FDA Adverse Event Reporting System (FAERS): Latest Quartely Data Files 24 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
CLIA Currently Waived Analytes 20 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
FDA Recognized Consensus Standards 17 recent views
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
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
Total Product Life Cycle (TPLC) 15 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 14 recent views
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
NHRIC (National Health Related Items Code) 13 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
Product Classification 11 recent views
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
FDA Pet Food Recalls 10 recent views
U.S. Department of Health & Human Services —
Contains data for FDA pet food recalls since January 1, 2006. -
Federal
MDR (Medical Device Reporting) 10 recent views
U.S. Department of Health & Human Services —
This database allows you to search the CDRH's database information on medical devices which may have malfunctioned or caused a death or serious injury during the... -
Federal
Clinical Investigator Inspector List (CLIIL)
U.S. Department of Health & Human Services —
The Clinical Investigator Inspection List (CLIIL) contains names, addresses, and other pertinent information gathered from inspections of clinical investigators who... -
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
Approved Animal Drug Products (Green Book)
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
FDA Data Inventory
U.S. Department of Health & Human Services —
An inventory of all FDA Datasets -
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
Premarket Notifications (510(k)s)
U.S. Department of Health & Human Services —
Medical device manufacturers are required to submit a premarket notification or 510(k) if they intend to introduce a device into commercial distribution for the first... -
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...
86 datasets found for "organization:((hhs-gov) OR (nlm-nih-gov) OR (cdc-hhs-gov) OR (acf-hhs-gov) OR (ahrq-hhs-gov) OR (cms-hhs-gov) OR (npdb-hrsa-gov) OR (aoa-hhs-gov) OR (hrsa-gov) OR (samhsa-hhs-gov) OR (fda-hhs-gov) OR (ihs-hhs-gov) OR (nih-hhs-gov))"