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USFDA

USFDA approval for J&J and Moderna C-19 booster dose

The US Food and Drug Administration (USFDA) has amended the emergency use authorisations (EUAs) for the Johnson & Johnson and Moderna C-19...
Medicine Capsule

Dr Reddy’s Lab gets USFDA nod for Lenalidomide capsule

Dr Reddy’s Laboratories today said it has received approval from the US health regulator to market Lenalidomide capsules, used to treat multiple...
USFDA

This drug becomes first FDA approved Nasal spray to treat dry eyes

(Reuters) - Oyster Point Pharma Inc's (OYST.O) treatment for dry eye disease became the first U.S. approved nasal spray for the chronic condition, sending...
USFDA

Don’t give yourself fillers with these Devices: FDA Says

The USFDA last week warned consumers not to use needle-free devices for injecting dermal fillers — which are promoted to the public...
Medicine Injection Vaccine

FDA panel endorse booster shot for J&J vaccine

US health advisers endorsed a booster of Johnson & Johnson’s C-19 vaccine Friday, citing concern that Americans who got the single-dose shot...
USFDA

USFDA advisers to review Merck’s Molnupiravir soon

A panel of outside advisers to the US health regulator will meet late next month to discuss whether to authorise Merck &...
Medicine Injection Vaccine

USFDA Staff: Moderna did not meet all criteria for booster dose

Scientists at the U.S. Food and Drug Administration (USFDA) said on Tuesday that Moderna Inc had not met all of the agency's criteria to support use...

FDA की टीम ने मेडिकल स्टोर पर की छापेमारी, मेडिकल सील: Haryana

FDA की टीम ने मेडिकल स्टोर पर की छापेमारी Haryana: Bahadurgarh शहर के सैनीपुरा में स्थित मेडिकल स्टोर...
USFDA

Merck and Ridgeback seek EUA from USFDA for Molnupiravir

Merck and Ridgeback Biotherapeutics yesterday announced that Merck has submitted an Emergency Use Authorisation (EUA) application to the US Food and Drug...
USFDA

Merck asks USFDA to authorize promising Anti Covid Pill

Drugmaker Merck asked U.S. regulators Monday to authorize its pill against COVID-19 in what would add an entirely new and easy-to-use weapon to the...
USFDA

USFDA gives tentative nod to Gland Pharma for generic muscle relaxant drug

Gland Pharma Limited, a generic injectable focused pharmaceutical company, received tentative approval from the United States Food and Drug Administration (USFDA) for...
USFDA

USFDA gives tentative nod to Zydus Cadila for Adapalene and Benzoyl Peroxide Gel

Zydus Cadila has received tentative approval from the US Food and Drugs Administration (USFDA) to market Adapalene and Benzoyl Peroxide Gel 0.3%/2.5%....
USFDA

USFDA gives nod to Drug to treat Rare Autoimmune Disease

ChemoCentryx Inc said on Friday the U.S. health agency approved its lead drug for treating a rare, fatal autoimmune disease, sending the biopharmaceutical...
Medicine Tablet

USFDA gives tentative nod to Lupin for generic Brexpiprazole tablets

Lupin yesterday said it has received tentative nod from the US health regulator to market generic Brexpiprazole tablets, which are used with...
FDA

FDA to launch prosecution against 77 Medical Stores

The Tamil Nadu Drugs Control Department is gearing up to launch prosecution against 77 medical stores belonging to all districts in the...
USFDA

FDA advisers to review C-19 shots for young kids

An advisory panel of experts to the U.S. drug regulator will hold meetings this month to review data on Pfizer Inc's C-19...
DCGI CDSCO

DCGI asks State FDAs to ensure uninterrupted supply of Medical Devices

The Drugs Controller General (India) has asked the State drug controllers of State FDAs of India to ensure uninterrupted supply of medical...
FDA

FDA to check food licenses of all street vendors

PUNE The Food and Drug Administration (FDA) will launch a drive to check if all eateries in the city have the necessary...
FDA

Maharashtra FDA issues stop sale order to 246 pharmacies

The Maharashtra Food and Drug Administration (FDA) has revealed that out of 3,460 inspections conducted on pharmacies in the state, as many...
USFDA

USFDA issues 6 observations to Biocon’s Malaysian facility

Biotechnology major Biocon on Saturday said the US health regulator has issued six observations after the inspection of the manufacturing facility of its Malaysian subsidiary Biocon Sdn Bhd....
USFDA

Zydus Cadila gets USFDA nod for drug to treat Psoriasis

NEW DELHI: Drug firm Zydus Cadila said it has received approval from the US health regulator to market Apremilast tablets, used to...
Documents of medical store

Amaris Clinicals completes USFDA Audit with NIL observations: Chennai

Amaris Clinicals, the clinical research organization (CRO) division of Caplin Point Laboratories Limited, located at Chennai, has completed a virtual audit from...
USFDA

Lupin gets these 7 observations from USFDA for Goa Plant

Pharma-major Lupin has received seven observations from the USFDA after the latter carried an inspection at the company's Goa facility in India.
USFDA

USFDA approves Pfizer booster shots only for people over 65

Washington: The US Food and Drug Administration advisory (USFDA) committee on Friday (local time) voted unanimously to authorize Pfizer booster shots for use in people aged...

Latest posts

NPPA releases draft of retail price calculation for 5 formulations

The National Pharmaceutical Pricing Authority (NPPA) has released draft version of proposed retail price calculation for five formulations, including a combination of...

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