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BE’S PNEUBEVAX 14TM SAFE & IMMUNOGENIC IN 6-8-WEEK OLD INFANTS

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Apr 30

MiracleMe Introduces Revolutionary Orally Dissolving Plant-Based Nutrition Products

Sourced from nature, backed by science. All products of Miracle Me is all about eating fruits & veggies the easy way....
Apr 18

FDA Greenlights Lupin's Varenicline Tablets: A Game-Changer in Smoking Cessation Therapy

Lupin Limited's FDA approval for its generic Varenicline tablets marks a significant milestone in the field of smoking cessation therapy....
Mar 18

Combatting Chikungunya: Valneva's Chikungunya Vaccine Cleared by USFDA, Eyes India Launch

As Valneva works towards making this groundbreaking vaccine available in India, the collaboration with CEPI and Instituto Butantan underlines the global effort to address infectious ...
Nov 16

Setting a New Standard in Patient Safety: Dozee Unveils ‘Dozee Pro Ex’ for Seamless Continuum of Monitoring from Hospital to Home

Dozee Pro Ex will offer Ambulatory patient monitoring for a seamless continuum of patient monitoring across different care settings ....
Oct 31

Mumbai's Medical Community Calls for Accountability and Quality in Drug Prescriptions

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Aug 17

Now get treatment of rare disease disorders like Duchenne Muscular Dystrophy with Hanugen Therapeutics

1 out of 3,500 boys will be affected by Duchenne muscular dystrophy (DMD), a rare genetic disorder that can get fatal. Affordable and accessible ...
Jul 26

A Holistic Ayurveda Platform For Men’s Health- AADAR AYURVEDA

Men are considered the head of the family. Working day and night they tend to neglect health. It's time to target men’s health. ...
Jun 28

US FDA approves Jardiance (empagliflozin) to treat adults living with heart failure with reduced ejection fraction

Latest Pharma News Update...
Aug 23

Zydus Cadila receives tentative approval from USFDA for Pemetrexed for Injection

Pemetrexed is used to treat certain types of cancers such as lung cancer, mesothelioma. It is a chemotherapy drug that works by slowing or stopping ...
Jun 25

Grace Science receives U.S. FDA orphan drug designation for GS-100, an AAV9 Gene Therapy for NGLY1 deficiency

Latest FDA drug approval update...
Jun 24

Zydus Cadila receives tentative approval from USFDA for Fingolimod Capsules .25mg

It is a sphingosine 1-phosphate receptor modulator indicated for the treatment of relapsing forms of multiple sclerosis (MS)....
Jun 24

Dr. Reddy's Laboratories announces the launch of Icosapent Ethyl Capsules, 1 gram in the U.S. Market

Dr. Reddy’s Icosapent Ethyl is available in 1 gram capsules in bottle count size of 120’s count....
Jun 22

Sun Pharma Announces Settlement of Patent Litigation for Generic Revlimid (lenalidomide) in US

The license will also allow Sun Pharma to manufacture and sell an unlimited quantity of generic lenalidomide capsules in the US beginning January 31, 2026....
Jun 22

Alembic Pharmaceuticals announces its joint venture Aleor Dermaceuticals receives USFDA Final Approval for Testosterone Topical Solution USP, 30 mg per pump actuation

Testosterone Topical Solution USP, 30 mg per pump actuation is indicated for replacement therapy in males for conditions associated with a deficiency or absence of ...
Jun 17

NATCO receives approval for Carfilzomib Vials ANDA (generic for KYPROLIS) in the US market

By virtue of the settlement, NATCO and Breckenridge have been granted a license permitting the launch of their generic carfilzomib products on a date that ...
Jun 14

Zydus Cadila receives tentative approval from USFDA for Brivaracetam Tablet

Brivaracetam is used to treat partial-onset of seizures (epilepsy)...
Jun 14

U.S. FDA expands approval of Pfizer’s LORBRENA as first-line treatment for ALK-Positive Metastatic Lung Cancer

In 2018, the FDA approved LORBRENA for the treatment of patients with ALK-positive metastatic NSCLC whose disease has progressed on crizotinib and at least ...
Mar 05

Sorrento receives USFDA clearance to start a clinical trial of Anti-CD47 antibody

Sorrento receives USFDA clearance to start a clinical trial of Anti-CD47 Antibody, discovered from fully human G-MAB library, for treatment of multiple malignancies ...
Mar 03

Johnson & Johnson's Covid-19 vaccine gets emergency use authorization from FDA

Johnson's vaccine is indicated for individuals above 18 years...
Mar 01

Strides receives USFDA approval for Ibuprofen OTC Oral Suspension

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Feb 24

Unichem received ANDA approval from USFDA for Apremilast Tablets

Another ANDA approval for Unichem Lab...
Feb 19

USFDA approves drug to reduce bone marrow suppression caused by chemotherapy

The new drug will give patients a treatment option that can reduce the occurrence of a common, harmful side effect of chemotherapy...
Feb 17

Lupin Launches Posaconazole Delayed-Release Tablets

Lupin & its AET Pharma US Inc. (part of Tiefenbacher Group) received an approval for its ANDA from the USFDA...
Feb 17

Forge Biologics receives USFDA fast track, orphan drug, and rare pediatric disease designations

Forge Biologics receives FDA fast track, orphan drug, and rare pediatric disease designations for FBX-101 gene therapy for patients with krabbe disease ...
Feb 17

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