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Welcome To IANS Live - BUSINESS - Glenmark Pharma launches Rufinamide tablets

In a statement issued Glenmark said it was one of the first Abbreviated New Drug Application (ANDA) applicants to submit a substantially complete ANDA for Rufinamide tablets.Comm

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Glenmark s consolidated revenues grow 2 8% to Rs 1,09,439 M in FY21

Glenmark s consolidated revenues grow 2.8% to Rs 1,09,439 M in FY21 Glenmark s consolidated revenues grow 2.8% to Rs 1,09,439 M in FY21 31 May 2021 | News Registers consolidated net profit of Rs 9,701 M with growth of 25 per cent in FY21 Image credit: Shutterstock.com Glenmark Pharmaceuticals announced its financial results for the fourth quarter and year ended March 31, 2021. For the fourth quarter of FY 2020-21, Glenmark s consolidated revenue was at Rs 28,599 million as against Rs 27,675 million recording an increase of 3.3 per cent. Consolidated EBITDA grew by 12.4 per cent to Rs 5,234 million in the quarter ended March 31, 2021 as against Rs 4,657 million in the previous corresponding quarter. The consolidated net profit was at Rs 2,339 million for the quarter ended March 31, 2021 as compared to Rs 2,203 million in the previous corresponding quarter, registering an increase of 6.2 per cent.

Glenn saldanhaGlenmark pharmaceuticalsPer shareGlenn saldanhaக்ளென் சால்தான்க்ளேண்மர்க் மருந்துகள்ஒன்றுக்கு பகிர்

Results: Glenmark Pharma Q4 net profit up 6% at Rs 233 87 cr

Results: Glenmark Pharma Q4 net profit up 6% at Rs 233 87 cr
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Glenn saldanhaGlenmark pharmaceuticalsPharmaceuticals chairmanGlenmark pharmaGlenmark pharma q4க்ளென் சால்தான்க்ளேண்மர்க் மருந்துகள்மருந்துகள் தலைவர்க்ளேண்மர்க் பார்மா

Lignocaine Market to Witness Revolutionary Growth by 2026 | AstraZeneca, Pfizer, Glenmark Pharma, Centura, Teligent

Lignocaine Market to Witness Revolutionary Growth by 2026 | AstraZeneca, Pfizer, Glenmark Pharma, Centura, Teligent

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Glenmark receives US FDA approval for Icatibant Injection

Glenmark receives US FDA approval for Icatibant Injection Glenmark receives US FDA approval for Icatibant Injection 25 May 2021 | News The injection will be manufactured in their North American manufacturing facility based in Monroe, North Carolina Glenmark Pharmaceuticals (Glenmark) has received final approval by the United States Food & Drug Administration (US FDA) for Icatibant Injection, 30 mg/3 mL (10 mg/mL) Single-Dose Prefilled Syringe, the generic version of Firazyr 1 Injection, 30 mg/3 mL (10 mg/mL) Single-Dose Prefilled Syringe, of Shire Human Genetic Therapies. This marks Glenmark s first synthetic decapeptide injectable approval and will be manufactured in their North American manufacturing facility based in Monroe, North Carolina.

United statesNorth carolinaGlenmark pharmaceuticalsUnited states food drug administrationUnited states foodDrug administrationIcatibant injectionSingle dose prefilled syringeShire human geneticNorth americanFirazyr injectionS fdaIcatibant injectionஒன்றுபட்டது மாநிலங்களில்வடக்கு கரோலினாக்ளேண்மர்க் மருந்துகள்