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Latest Articles in zydus cadila

Talks On To Make Zydus Cadila's COVID-19 DNA Vaccine Part Of Inoculation Programme: Govt

Zydus Cadila's indigenously-developed needle-free COVID-19 vaccine ZyCoV-D received the Emergency Use Authorisation from the Drugs Controller General of India last month and will be administered to those aged 12 years and above.

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Zydus Cadila Gets USFDA Nod To Market Depression Treatment Drug In US Market

The drug will be manufactured at the group''s formulation manufacturing facility at the SEZ, Ahmedabad, Zydus Cadila noted.

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Zydus Cadila Gets USFDA Nod For Diabetes Medication

Zydus had filed a new drug application (NDA) with the USFDA seeking approval to market Sitagliptin base 25, 50 and 100 mg tablets.

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Zydus Cadila's COVID-19 Vaccine Can Be Available From First Week Of October

Covishield, Covaxin and Sputnik V vaccines are being given to only those above 18 years and unlike ZyCoV-D, which is three-dose, these are administered in two doses.

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Zydus Cadila Gets USFDA Nod For Arthritis Drug With 180-Days Exclusivity

Zydus was the first abbreviated new drug application (ANDA) filer on Tofacitinib extended-release tablets 22 mg and thus holds 180-day exclusivity on this strength

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Hope To Start Supply of ZyCoV-D Vaccine By Mid To End Sept: Zydus Group MD

Asked if the company was considering partnering with other firms to scale up production of its vaccine, Patel said Zydus Cadila is actively looking at ramping up manufacturing both domestically through partnerships and also outside of the country.

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Zydus Cadila Gets USFDA Nod For Breast Cancer Treatment Drug

The group now has 320 approvals and has so far filed over 400 abbreviated new drug applications (ANDAs) since the commencement of the filing process in FY 2003-04.

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Zydus Cadila Gets Tentative Nod From USFDA To Market Cancer Drug

The drug will be manufactured at the group's formulation manufacturing facility at the SEZ, Ahmedabad

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Zydus Cadila Applies For Emergency Use Nod For COVID-19 Vaccine

An approval for Zydus' vaccine, ZyCoV-D, would make it the fifth vaccine authorized for use in India, after Moderna, AstraZeneca (AZN.L) and partner Serum Institute of India's Covishield, Bharat Biotech's Covaxin, and Sputnik V developed by Russia's Gamaleya Institute.

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Zydus Cadila Gets USFDA Approval For Generic Cancer Drug

The group now has 319 approvals and has so far filed over 400 abbreviated new drug applications (ANDAs) since the commencement of the filing process in 2003-04

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Zydus Cadila Gets Tentative USFDA Nod To Market Generic Sclerosis Treatment Drug

The company has received tentative approval from the US Food and Drug Administration (USFDA) to market the product in the strength of .25 mg

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Zydus Cadila Gets USFDA Tentative Nod For Epilepsy Treatment Drug

The group now has 319 approvals and has so far filed over 400 abbreviated new drug applications (ANDAs) since the commencement of the filing process in FY 2003-04.

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Zydus Cadila Gets Tentative USFDA Nod To Market Lung Cancer Treatment Drug

The group now has 318 approvals and has so far filed over 400 abbreviated new drug applications since the commencement of the filing process in financial year 2003-04.

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Zydus Cadila Gets USFDA Nod For Cancer And High Blood Pressure Treatment Drug

Zydus Cadila has received final approval from the US Food and Drug Administration (USFDA) to market Ibrutinib Capsules in the strengths of 70 mg and 140 mg, Cadila Healthcare said in a regulatory filing.

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Zydus Cadila Seeks DCGI Nod For Use Of Hepatitis Drug For COVID-19 Treatment

The interim results indicate that the drug when administered early on, could help patients recover faster and avoid much of the complications seen in the advanced stages of the disease

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