- U. S. Food and Drug Administration
The FDA is responsible for protecting the public health by ensuring the safety, efficacy, and security of human and veterinary drugs, biological products, and medical devices; and by ensuring the
- Food and Drug Administration (FDA) | USAGov
The Food and Drug Administration (FDA) is responsible for protecting the public health by assuring the safety, efficacy, and security of human and veterinary drugs, biological products, medical devices, our nation's food supply, cosmetics, and products that emit radiation
- Food and Drug Administration - Wikipedia
The United States Food and Drug Administration (FDA or US FDA) is a federal agency of the Department of Health and Human Services
- FDA Dashboards - Home
The Data Dashboard contains data elements from FDA compliance and enforcement data sources, including Inspections, Compliance Actions, Recalls, Imports, and Food Safety Modernization Act
- 510 (K) Premarket Notification - Food and Drug Administration
A 510 (K) is a premarket submission made to FDA to demonstrate that the device to be marketed is as safe and effective, that is, substantially equivalent, to a legally marketed device (section
- Drugs@FDA - Food and Drug Administration
Drugs@FDA includes most of the drug products approved since 1939 The majority of patient information, labels, approval letters, reviews, and other information are available for drug products
- FDALabel - U. S. Food and Drug Administration
FDALabel, NCTR Drug Label Search ApplicationInitial U S Approval [4 Digit Year] (23401 labeling) Highlights [Excluding Product Title] (23432 labeling) 8 3 Females and Males of Reproductive Potential (2807 labeling) 13 1 Carcinogenesis, Mutagenesis, Impairment of Fertility (33501 labeling) 13 2 Animal Toxicology and or Pharmacology (6153 labeling) 16 HOW SUPPLIED STORAGE AND HANDLING (84015
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