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Purpose: The stability of sildenafil citrate 2.5 mg/mL in two extemporaneously prepared oral suspensions stored at 4 and 25 ºC was studied. Methods: Thirty 25-mg tablets of sildenafil citrate ...
Kerala Infrastructure and Technology for Education (KITE), the technology wing of the State’s General Education department, has distributed 29,000 robotic kits in high schools across Kerala ...
Ludhiana: A boy died of an electric shock while trying to get back his kite, which got stuck in electrical wires, at Malak village in Jagraon. The deceased was identified as Ekamjit Singh ...
Indoco Remedies Limited, a fully integrated, research-oriented pharmaceutical company, announced the receipt of final approval from the US FDA for Abbreviated New Drug Application (ANDA) for ...
Heat 200 mL of purified water, USP, to boiling ... until the solution is clear and homogeneous. Place 30 25-mg sildenafil citrate tablets into a mortar and reduce to a fine powder.
“Kite Man: Hell Yeah!,” premiering Thursday on Max, keeps the nervy lewdness and contemporary pop-psychology of “Harley” but redirects its energy to Kite Man (voiced by Matt Oberg).
"We fly kites instead of warplanes," 13-year-old Hala Fayyad said. GAZA -- Hala Fayyad is proud of her handmade kite, decorated in the colors of the Palestinian flag. The four pieces of colored ...
Study will compare bioavailability of Sildenafil Oral Suspension and Viagra® tablets under fasted conditions Companion study will evaluate the effects of food on the bioavailability of Sildenafil ...
ANI’s Estradiol Tablets USP are the generic version of the Reference Listed Drug (RLD) Estrace ®. The According to IQVIA, a leading healthcare data and analytics provider, the current annual U ...
CMP Pharma, a pharmaceutical manufacturer, announced that Liqrev, the first FDA-approved ready-made oral liquid of sildenafil, is now available. Created for patients with the inability to swallow ...
--(BUSINESS WIRE)--ANI Pharmaceuticals, Inc. (ANI or the Company) (Nasdaq: ANIP) today announced that it received U.S. Food and Drug Administration (FDA) approval for the Abbreviated New Drug ...
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