Approved active drugs with sponsors to which FDA has granted exclusivity for pediatric studies under Section 505A of the Federal Food, Drug, and Cosmetic Act (FD&C Act)
Similar Posts
List of Off-Patent, Off-Exclusivity Drugs without an Approved Generic
The FDA maintains a list of approved new drug application (NDA) drug products that are no longer protected by patents or exclusivities, and for which the FDA has not approved an ANDA referencing that NDA drug product.Unico Holdings, Inc., Lake Worth, FL 483 issued 2/14/2006
Unico Holdings, Inc., Lake Worth, FL 483 issued 2/14/2006Primavera Nueva Inc. Issues Voluntary Recall of Select 4-Count Tamales Because of Possible Health Risk- Revised to Include Roasted Pumpkin & White Cheddar, a Seasonal Item
Sonoma, CA — Primavera Nueva Inc. is voluntarily recalling certain lots of its 4-count tamales because the products have the potential to be contaminated with Listeria monocytogenes, an organism whichHiding in Plain Sight: 7-OH Products
7-OH: Emergence of a Fourth Opioid EpidemicBlack Horse Miracle Honey for Men may be harmful due to hidden drug ingredients
The Food and Drug Administration is advising consumers not to purchase or use Black Horse Miracle Honey for Men, a product promoted and sold for sexual enhancement on various websites and possibly in some retail stores.Safe Use Initiative – Current Projects
Part of Safe Use Initiative
(updated)
