Pharma
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6.5KZydus receives USFDA nod for dementia drug
Pharmaceutical major Zydus Cadila has received final approval from the US Food and Drug Administration (USFDA) to market Donepezil Hydrochloride tablets in...
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6.2KAjanta Pharma announces launch of migraine drug in US
Indian pharmaceutical company Ajanta Pharma Limited has announced the launch of Eletriptan Hydrobromide tablets (20 mg and 40 mg) in the US...
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2.8KZydus gets final USFDA nod for Aspirin, anti-blood clotting drug
Indian pharmaceutical major Zydus Cadila has received the final approval from the United States Food and Drug Administration (USFDA) to market Aspirin,...
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5.6KIbuprofen raises risk of heart disease, stroke in arthritis sufferers: Report
Arthritis sufferers who take the drug ibuprofen for pain relief are at greater risk of high blood pressure, heart disease and stroke,...
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3.9KZydus Cadila receives two USFDA approvals
Pharma major Zydus Cadila on Wednesday announced to have received USFDA nod to market Tiadylt ER capsule and Azelastine Hydrochlorid Nasal spray...
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3.2KLupin gets USFDA nod for cholesterol drug
Drug firm Lupin has received FDA approval to market Nikita aka Pitavastatin tablets ”used for lowering bad cholesterol levels, available in 1 mg, 2...
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8.1KDCGI nod to Mylan for marketing HIV drug in India
The Drug Controller General of India (DCGI) has given a green signal to global pharma firm Mylan for marketing its antiretroviral (ARV)...
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5.2KGlenmark Pharmaceuticals receives ANDA approval for anti-herpes ointment
Glenmark Pharmaceuticals has received the final ANDA approval from the United States Food and Drug Administration (USFDA) to market Acyclovir ointment USP...
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5.5KAlembic Pharma receives USFDA approval for anti-bacterial drug
Alembic Pharmaceuticals Limited on Monday announced that it has received approval from the US Food and Drug Administration (USFDA) for its Abbreviated...
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7.4K
Zydus Cadila gets USFDA nod for colitis tablets
US Food and Drug Administration (FDA) has given its nod to Indian pharmaceutical major Zydus Cadila for manufacturing of Mesalamine Delayed-Release Tablets...
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6.6KNatco Pharma receives successful EIR from USFDA for its Telangana unit
Indian pharmaceutical company Natco Pharma Limited has received successful Establishment Inspection Report (EIR) from the US Food and Drug Administration (USFDA) for...
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6.2KWhat would it take to push Indian pharma sector on growth path?
India has been doing exceptionally well in the pharmaceutical sector for the last 20-25 years, but since the country agreed to comply...
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5.4KGlenmark gets USFDA approval for hypertension and high BP drugs
Glenmark Pharmaceuticals on Friday announced that the leading research“based global pharmaceutical company has been granted final Abbreviated New Drug Application (ANDA) approval...
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