1. What is the Chemxpert database?

Chemxpert database is a techno-commercial information platform developed and operated by Lifescience Intellipedia Pvt. Ltd. Our data provides valuable insights regarding sourcing, marketing, development, and regulatory functions for the entire Lifescience industry. The different industries covered by our data encompass APIs, FDFs, pharma intermediates, paints, dyes, polymers, biotechnology, biochemical, food additives, nutraceuticals, etc.

2. How can I subscribe to the Chemxpert database?

You can gain access to the Chemxpert database after subscribing to it by visiting this link: - https://chemxpert.com/pricing

3. How many countries' data is available on your portal?

The Chemxpert database covers more than 200 countries. We are working in the direction of expanding our data coverage in more countries.

4. What are the different sources you use for obtaining information?

The different sources we use for data collection are as follows: - • Primary researc • DMF, ANDA, & CEP list • Conferences, Exhibitions, & Tradeshow • Company annual reports • DMF, ANDA, & CEP list • Subject matter experts & KOL survey. Apart from these, our other valuable sources include application-wise manufacturers list, subscribed and non-subscribed databases, corporate partners, US FDA Orange book, publicly available sources, industry associates, national statistics, regulatory websites, etc. You can gain access to the Chemxpert database after subscribing to it by visiting this link: -https://chemxpert.com/sources

5. What is the expected time for account activation?

Your Chemxpert account will be activated instantly if the payment is made through our website. If you choose to use RTGS, NEFT, or IMPS systems for payment, your account will be activated within 24 hours.

04 Oct 2022
Admin
News Article

Zydus Lifesciences Gets Usfda Nod For Generic Drug

Zydus Was One Of The First Applicants To Submit A Substantially Complete Anda (Abbreviated New Drugs Application) With A Paragraph Iv Certification For Mirabegron Extended-Release Tablets, 25 Mg And 50 Mg And I, Therefore,E Eligible For 180 Days Of Shared Generic Drug Exclusivity For The DrugZydus Lifesciences On Monday Said It Has Received The Usfda'S Final Nod To Market Its Generic Version Of Mirabegron Extended-Release Tablets Used To Treat Overactive Bladder, With 180 Days Of Shared Generic Drug Exclusivity. The Final Approval Granted By The Us Food And Drug Administration (Usfda) To The Company'S Us Arm Zydus Pharmaceuticals Inc Is For The Tablets Of Strengths 25 Mg And 50 Mg, It Said In A Regulatory Filing. Zydus Was One Of The First Applicants To Submit A Substantially Complete Anda (Abbreviated New Drugs Application) With A Paragraph Iv Certification For Mirabegron Extended-Release Tablets, 25 Mg And 50 Mg And I, Therefore,E Eligible Mirabegron Zydus Pharmaceuticals Inc Zydus Drug For Mirabegron Health News For 180 Days Of Shared Generic Drug Exclusivity For The Drug, It Added

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