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Lupin receives Tentative Approval for Generic Glumetza® Extended-Release Tablets - Lupin | Press Release
1+ mon, 3+ week ago (25+ words) Lupin receives Tentative Approval for Generic Glumetza" Extended-Release Tablets - Lupin | Press Release'lupin.com Lupin receives Tentative Approval for Generic Glumetza" Extended-Release Tablets...
Primal Herbs supplement recalled after FDA analysis finds undeclared active ingredient in Viagra
2+ week, 4+ day ago (27+ words) Primal Herbs supplement recalled after FDA analysis finds undeclared active ingredient in Viagra...Viagra'ABC7 New York Herbal supplement recalled after FDA analysis finds undeclared active ingredient in Viagra...
Lupin gets tentative US FDA approval for Sertraline - Lupin | Press Release
1+ mon, 3+ week ago (21+ words) Lupin gets tentative US FDA approval for Sertraline - Lupin | Press Release'lupin.com Lupin gets tentative US FDA approval for Sertraline...
Ask Your Pharmacist: What is generic medication?
1+ mon, 1+ week ago (107+ words) saved articles in your account and clicking the X located at the bottom right of the article....
Pharmalittle: We're reading about TrumpRx, Hims & Hers selling compounded Wegovy pill, and more
1+ mon, 3+ week ago (495+ words) worked at The Wall Street Journal, The Star-Ledger of New Jersey, and New York Newsday, among other publications....finalist in explanatory journalism in 2016 for a series of stories on prescription drug pricing. He earned an...industry for nearly three decades....
Legislative Push for FDA Preemptive Authority Over Dietary Supplement Regulation
1+ mon, 2+ week ago (427+ words) Legislative Push for FDA Preemptive Authority Over Dietary Supplement Regulation'The National...clarify and affirm the Food and Drug Administration's (FDA) preemptive authority over dietary supplement regulation....successfully applies for a specific exemption from FDA preemptive authority. Such exemptions would be…...
Savara Highlights FDA Priority Review for Molbreevi as Aug. 22 PDUFA Date Nears
1+ mon, 19+ hour ago (521+ words)FDA has accepted and filed Savara's BLA for Molbreevi in autoimmune PAP, granted priority review, and set a PDUFA date of Aug. 22; Savara also expects to file MAAs in the EU and U.K. by the end of March. Data from the…...
Supplement Industry Seeks FDA Approval for Peptides and New Ingredients
6+ day, 9+ hour ago (896+ words) AM Dietary supplement manufacturers are urging the FDA to broaden ingredient regulations to include peptides,...nation's top health official, has pledged to reduce FDA restrictions on these products. On Friday, the Food...protection groups, and researchers. This marks the…...
Lupin receives tentative US FDA Approval for Ziprasidone - Lupin | Press Release
1+ mon, 3+ week ago (21+ words) Lupin receives tentative US FDA Approval for Ziprasidone - Lupin | Press Release'lupin.com Lupin receives tentative US FDA Approval for Ziprasidone...
Tylenol, Advil, Purina, Haribo face urgent FDA recall
2+ mon, 4+ week ago (633+ words) single food or beverage, or pet-food product, because of a recall. Hundreds of food recalls happen each year so they can be hard to keep track of, even though I follow the FDA's recall notice page and read about…...