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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
Food and Drug Administration--Recalls
U.S. Department of Health & Human Services —
This feed describes all new items that are being recalled by the FDA. -
Federal
FDA Online Label Repository
U.S. Department of Health & Human Services —
The drug labels and other drug-specific information on this Web site represent the most recent drug listing information companies have submitted to the Food and Drug... -
Federal
Recalls of Food and Dietary Supplements
U.S. Department of Health & Human Services —
Food producers recall their products from the marketplace when the products are mislabeled or when the food may present a health hazard to consumers because the food... -
Federal
FDA Pet Food Recalls
U.S. Department of Health & Human Services —
Contains data for FDA pet food recalls since January 1, 2006. -
Federal
NHRIC (National Health Related Items Code)
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
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
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
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
MedSun Reports
U.S. Department of Health & Human Services —
The Medical Product Safety Network (MedSun) is an adverse event reporting program launched in 2002. The primary goal for MedSun is to work collaboratively with the... -
Federal
CFSAN Web Modules
U.S. Department of Health & Human Services —
This system shares public data that can be downloaded. -
Federal
Liothyronine sodium
U.S. Department of Health & Human Services —
Liothyronine Sodium is a generic prescription medication used to treat thyroid hormone deficiency (hypothyroidism). It comes as oral tablets in strengths of 0.005 mg,... -
Federal
Metronidazole oral
U.S. Department of Health & Human Services —
LIKMEZ is a prescription oral suspension containing metronidazole, an antibiotic that treats infections caused by certain bacteria and parasites. Each 5 mL provides... -
Federal
Code of Federal Regulations Title 21
U.S. Department of Health & Human Services —
This database contains the most recent revision from the Government Printing Office (GPO) of the Code of Federal Regulations (CFR) Title 21 - Food and Drugs. -
Federal
Dorzolamide hydrochloride and timolol maleate preservative free
U.S. Department of Health & Human Services —
Dorzolamide Hydrochloride and Timolol Maleate is a preservative-free ophthalmic solution (eye drops) used to lower intraocular pressure in patients with glaucoma or... -
Federal
IVD Home Use Lab Tests (Over The Counter) Tests
U.S. Department of Health & Human Services —
Searchable listing of Over-the-Counter tests (OTC) and collection kits that have been cleared or approved by the FDA -
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
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
Testosterone cypionate
U.S. Department of Health & Human Services —
Testosterone Cypionate is a prescription injectable solution used to supplement testosterone levels in men with low hormone production. It is administered... -
Federal
Ustekinumab
U.S. Department of Health & Human Services —
Stelara (ustekinumab) is a prescription biologic medication that blocks interleukin-12 and interleukin-23 to reduce inflammation. It's given as subcutaneous...