Por: RTTNews Health September 06, 2023
Amneal Pharmaceuticals, Inc. () announced Wednesday it has received Abbreviated New Drug Application (ANDA) approval from the U.S. Food and Drug Administration for lisdexamfetamine dimesylate capsules, 20 mg, 30 mg, 40 mg, 50 mg, 60 mg, and 70 mg.Lisdexamfetamine dimesylate capsules is a generic version of Vyvanse. This ADHD product is currently on the U.S. FDA shortage product list, and Amneal has already begun supplying product to the... + full article
RTTNews USA Health September 06, 2023
Brooklyn, New York-based WEFUN Inc is recalling 300 boxes of dietary supplement capsules to the consumer level for undeclared Sildenafil, the U.S. Food and Drug Administration said.Sildenafil is an ingredient known as a Phosphodiesterase Inhibitor or PDE-5 inhibitor found in... + más
Alzheimer's Q&A: Sildenafil has potential as Alzheimer's drug | The Advocate
RTTNews USA Health August 31, 2023
Mallinckrodt plc announced its Specialty Generics segment, operating as SpecGx, received approval from FDA for its Abbreviated New Drug Application for Lisdexamfetamine Dimesylate Capsules 10mg, 20mg, 30mg, 40mg, 50mg, 60mg, and 70mg. The FDA found SpecGx LLC's product was... + más
ADHD Medication Might Help In Treating Amphetamine Addiction | Forbes
Chemical company to pay more than $185 million to remove mercury from Penobscot River | Portland Press Herald
RTTNews USA Health July 05, 2023
Amneal Pharmaceuticals, Inc. () said the company has received a Complete Response Letter from the FDA regarding the New Drug Application for IPX203 for the treatment of Parkinson's disease. The letter stated that although an adequate scientific bridge was established for... + más
High school scores and top performers from Friday, March 24 | Orlando Sentinel
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RTTNews USA Health June 15, 2023
Harvard Drug Group, LLC d/b/a Major Pharmaceutical and Rugby Laboratories is recalling a single lot of Dronabinol Capsules, USP, 2.5 mg and Ziprasidone Hydrochloride Capsules, 20 mg. The packaging may contain incorrect product due to labeling mix-up, the U.S. Food and Drug... + más
Aurobindo Pharma Recalls Quinapril And Hydrochlorothiazide Tablets | RTTNews
Amneal Pharma Says FDA Accepts For Review ANDA For Naloxone Hydrochloride Nasal Spray | RTTNews
RTTNews USA Health May 15, 2023
ANI Pharmaceuticals, Inc. () announced Monday that it received U.S. Food and Drug Administration (FDA) approval for the Abbreviated New Drug Applications (ANDAs) for Methsuximide Capsules USP, 300 mg and Alendronate Sodium Oral Solution 70 mg (base)/75 mL.Methsuximide Capsules... + más
‘Luckiest Girl Alive’ Is Trauma on Trauma | Vanity Fair
‘Luckiest Girl Alive’ review: A woman’s trauma becomes a Netflix revenge saga starring Mila Kunis | Orlando Sentinel
ABC News USA Life February 04, 2023
Two types of artificial tears eye drops have been voluntarily recalled following 55 reports of adverse use effects, including eye infections, vision loss and even a bloodstream infection that led to one death, according to federal officials.The affected eye drops were... + más
Eye drops recalled after 55 reports of bacterial infection, 1 death in 12 states | ABC7
EzriCare recalls artificial tear drops after reports of vision loss and 1 death | CBS News
Forbes USA Tech November 26, 2022
A mock methamphetamine lab for teaching purposes at the new National Clandestine Laboratory Training ... [+] and Research Facility December 5, 2008 at the DEA Training Academy in Quantico, Virginia. Since 1987, DEA has trained over 19,000 officials to operate safely in... + más
For Some Women With ADHD, TikTok Is the First Place They Felt Heard | Time
Caffeine searches spike after FDA announces nationwide Adderall shortage | Newsweek
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