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Strides gets USFDA nod for potassium chloride for oral solution

Strides gets USFDA nod for potassium chloride for oral solution March 15, 2021 × Strides Pharma Science Limited (Strides) has announced that its step-down wholly-owned subsidiary, Strides Pharma Global Pte Limited, Singapore, has received approval for Potassium Chloride for Oral Solution USP, 20 mEq from the United States Food & Drug Administration (USFDA). The product is bio-equivalent and therapeutically equivalent to the Reference Listed Drug (RLD), Potassium Chloride for Oral Solution USP, 20 mEq, of Pharma Research Software Solution, LLC. Potassium chloride oral solution is indicated for the treatment and prophylaxis of hypokalemia with or without metabolic alkalosis, in patients for whom dietary management with potassium-rich foods or diuretic dose reduction are insufficient.

autoimmune hemolytic anemia treatment Market is Projected to Grow Massively in Near Future – KSU

The  autoimmune hemolytic anemia treatment Market research report thoroughly explains each and every aspect related to the Global autoimmune hemolytic anemia treatment Market, which facilitates the report’s reader to study and evaluate the upcoming market trend and execute the analytical data to promote the business. autoimmune hemolytic anemia treatment Market Insight: Global Autoimmune hemolytic anemia Treatment Market is growing at a steady CAGR in the forecast period of 2019-2026. Increasing research and development expenses and high demand of novel therapies are some factors fueling the market growth Avail Your Free Sample Copy of the autoimmune hemolytic anemia treatment Market Report (Including Full TOC, List of Tables & Figures, Chart)@ https://www.databridgemarketresearch.com/request-a-sample/?dbmr=global-autoimmune-hemolytic-anemia-treatment-market

Strides Pharma receives approval for ibuprofen from USFDA

Strides Pharma Science receives USFDA approval for Ibuprofen Oral Suspension

Strides Pharma Science announced that its step-down wholly owned subsidiary, Strides Pharma Global, Singapore, has received approval for Ibuprofen Oral Suspension USP,100 mg/5 mL (OTC) from the United States Food & Drug Administration (USFDA). The product is bioequivalent and therapeutically equivalent to the Reference Listed Drug (RLD), Children s Motrin Oral Suspension, 100 mg/mL, of Johnson & Johnson Consumer Inc. Strides is focusing on building a private label business in the US by leveraging its portfolio of products across soft gels, tablets, capsules, topicals, powders and oral solutions. Ibuprofen Oral Suspension USP,100 mg/5 mL (OTC) further strengthens company s private label portfolio for the US market. According to IRi data, the US market for Ibuprofen Oral Suspension USP,100 mg/5 mL (OTC) is

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