FDA data explorer

Every openFDA database, in one search.

30 datasets, 56,954,218 records: approvals, labels, NDCs, shortages, recalls, adverse event reports, device clearances and UDIs, substances, complete response letters and more. openFDA exported the newest on 2026-11-13.

“semaglutide” matches in 11 of 26 searchable datasets. 15 did not answer this time (Drug recalls, Device classification, 510(k) clearances, PMA approvals, Establishments and listings, Device recalls, Device recall enforcement reports, Unique device identifiers (GUDID), COVID-19 serology test evaluations, Cosmetic adverse event reports, Food recalls, Tobacco product problem reports, NDC SPL data elements, Historical FDA documents, Complete response letters); try again shortly.

Drugs

Orange Book 29

  • WEGOVY HD

    SEMAGLUTIDE · 7.2MG/0.75ML (7.2MG/0.75ML) · SOLUTION · SUBCUTANEOUS

    NDA215256HUMAN PRESCRIPTION DRUGReference listed drug
    FDA page
  • WEGOVY

    SEMAGLUTIDE · 1MG/0.5ML (1MG/0.5ML) · SOLUTION · SUBCUTANEOUS

    NDA215256HUMAN PRESCRIPTION DRUGReference listed drug
    FDA page
  • WEGOVY

    SEMAGLUTIDE · 1.7MG/0.75ML (1.7MG/0.75ML) · SOLUTION · SUBCUTANEOUS

    NDA215256HUMAN PRESCRIPTION DRUGReference listed drug
    FDA page
All 29 in Orange Book →

NDC directory 142

  • Semaglutide

    Semaglutide · Hybio Pharmaceutical Co., Ltd. · POWDER

    14403-0030BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDINGBulk ingredient
  • semaglutide

    semaglutide · Arene Life Sciences Private Limited · POWDER

    71859-010BULK INGREDIENTBulk ingredient
  • Semaglutide

    Semaglutide · Hybio Pharmaceutical Co., Ltd · POWDER

    14403-0030BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDINGBulk ingredient
All 142 in NDC directory →

Devices

Food

Food and supplement adverse event reports (CAERS) 4

All 4 in Food and supplement adverse event reports (CAERS) →

Animal & veterinary

Substances & reference

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Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.