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Which Artificial Sweeteners Are Approved By the FDA?
and other low-sugar or sugar-free products. Other zero- or low-calorie sweeteners that are natural like stevia, monk fruit extract, and many others are FDA-approved but they aren’t considered ...
Eli Lilly's tirzepatide is off the FDA's shortage list: What it means for patients
Eli Lilly's weight-loss drug is no longer on the Food and Drug Administration's drug shortage list. Compounding pharmacies ...
FiercePharma8d
In win for compounders, FDA will review its decision to put Eli Lilly's tirzepatide on shortage list
In accepting the FDA’s motion, U.S. District Judge Mark Pittman put on hold a lawsuit filed by the Outsourcing Facilities ...
pharmaphorum1d
Copaxone first on FDA's list for faster complex generic approvals
The approval is also significant for a host of other 'complex generic' products in the US, with the FDA announcing measures to reduce barriers to their approval. Shares in Teva ticked down on the ...
CBS News19d
FDA now weighing approval of first new sunscreen ingredient in decades
If the FDA agrees with DSM-Firmenich's request, the next step will be for the FDA to propose adding bemotrizinol to the list of over-the ... "Consumers are purchasing products with bemotrizinol ...
Nasdaq14d
Indivior Announces FDA Grants Priority Review For SUBLOCADE Prior Approval Supplement
(INDV) announced that the U.S. Food and Drug Administration has granted Priority Review designation for the Prior Approval Supplement of ... means that the FDA's goal is to take action on an ...
Drugmakers can keep making off-brand weight-loss drugs as FDA backpedals
Facing a lawsuit, the Food and Drug Administration has decided to reconsider its decision to take popular weight-loss and diabetes drugs off of the national shortage list, which will allow compounding ...
Morningstar27d
Heron Therapeutics Announces FDA Approval of the Prior Approval Supplement Application for ZYNRELEF® Vial Access Needle ("VAN")
today announced that the U.S. Food and Drug Administration (the "FDA") has approved the Company's Prior Approval Supplement Application for ZYNRELEF® (bupivacaine and meloxicam) extended-release ...
JD Supra14d
GLP-1 Drugs: FDA Removes Lilly’s Zepbound® and Mounjaro® (tirzepatide injection) from its Drug Shortage List
On October 2, 2024, the U.S. Food and Drug Administration (FDA) determined the shortage of the tirzepatide injection, a glucagon-like peptide ...
Pharmabiz26d
US FDA approves Heron Therapeutics’ prior approval supplement application for Zynrelef vial access needle
Heron Therapeutics, Inc., a commercial-stage biotechnology company, announced that the US Food and Drug Administration (FDA) has approved the company's Prior Approval Supplement Application for ...