This FDA approval from November 1983 represents a foundational milestone in Novartis's historical portfolio, though the current market impact is negli...
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# FDA Approves Hospira's Phytonadione (Vitamin K1) for Intramuscular Injection Hospira, Inc. received FDA approval for phytonadione (Vitamin K1) inje...
# FDA Approves GlaxoSmithKline Drug (NDA 018342) GlaxoSmithKline has received FDA approval for a new drug application, marking an expansion of the co...
Hospira has obtained regulatory approval for a listed product application, signaling continued expansion of its pharmaceutical portfolio despite the f...
# FDA Approval Newswire AbbVie Inc.'s DEPAKOTE (divalproex sodium) received FDA approval on March 10, 1983, establishing a foundational anticonvulsan...
# FDA Approves Methadone Hydrochloride Oral Formulation for Hikma Pharmaceuticals Hikma Pharmaceuticals USA Inc. received FDA approval for its oral m...
SUN PHARM INDUSTRIES announced FDA approval for ANDA087794, a regulatory milestone expected to bolster its product portfolio and support market share ...
The FDA has confirmed the approval of Marlex Pharmaceuticals' oral furosemide product, supporting a staple in acute treatment protocols. While not a n...
PAI Holdings, LLC dba PAI Pharma secured FDA approval for its Acetaminophen and Codeine Phosphate oral generic, strengthening the company’s position i...
Pharmobedient has announced approval for its ANDA submission, a milestone expected to drive market expansion for its generic product portfolio....
Hikma Pharmaceuticals USA Inc. announced this morning that the FDA approved a supplemental ANDA for Methadone Hydrochloride Oral Solution, a generic f...
# FDA Approves ICU Medical's Lactated Ringer's Solution, Expanding Critical Care Portfolio ICU Medical, Inc. has received FDA approval for Ringers (s...
HIKMA is positioned to bolster its market share following the FDA's approval of ANDA087003, a move expected to expand revenue streams as the generic e...
Sun Pharmaceutical Industries Ltd received FDA approval for an Abbreviated New Drug Application, a milestone that is poised to enhance the company's m...
Sun Pharma Industries Ltd. obtained FDA approval for Abbreviated New Drug Application 085868, marking a key regulatory advancement for a new generic p...
Actavis Mid Atlantic received FDA approval for a generic medication via ANDA #085861, strengthening its market position to capitalize on growth opport...
OZANTRI has solidified its market position in the pharmaceutical sector following the FDA's confirmation of its regulatory status via the benchmark AN...
# FDA Approves Organon's SINEMET (Carbidopa and Levodopa) for Oral Administration Organon LLC's approval of SINEMET, a combination of carbidopa and l...
FDA approved IMPAX LABS' Abbreviated New Drug Application (ANDA060469) on July 13, 1971, giving the company regulatory clearance to manufacture a gene...
Baxter Healthcare Corporation’s continued FDA validation of its Dextrose Monohydrate product reinforces the manufacturer’s dominant position in the in...