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exportapi@rlggroup.co.in
We are offering Ibuprofen BP/USP/EP/JP ( 15687-27-1) with a capacity to manufacture 3600 MT annually and have all the required documents, licenses and certifications. We have GMP, WHO-GMP, Wriiten Confirmation(WC), Halal Cerification, CEP-Application No- 2022-112 (expected to receive in next 2 months), DMF and other ISO licenses. Contact us on below details.
Ms Shikha Chandra
+91 90548 82176(Call/WhatsApp)
exportapi@rlggroup.co.in
vishvesh.shaishav@gmail.com
We are focussed on developing new manufacturing technologies, including custom synthesis of new moleculepharma intermediate, catalyst, bulk drugs, pharma API, pharma chemicals, active pharmaceutical ingredients, pharmaceutical pellets,additives, contract manufacturing, chemicals. We began in the field of specialty intermediates for pharmaceutical applications and developed our own purification technologies for manufacturing highly pure intermediates. And Pharmaceutical API At a later stage, we integrated forward to manufacture finished formulations for both veterinary and human consumption. Due to our completely integrated operations in the pharmaceutical sector, we continuously learn about the quality parameters for an API based on the performance of the finished formulation in order to quality their Bioequivalence Studies.?We have established finished formulation lines in South Asian and Latin American countries. It is our vision to achieve worldwide recognition as an excellent business partner from India by providing our customers with superior quality products at highly affordable prices and following that up with reliable service consistently, thereby giving them an unparalleled experience.?Our focus lies in developing new production technologies with a keen interest in frugal innovation in order to gain a competitive edge over others. We specialize in the custom synthesis of molecules and work with many reputed companies around the world on an OEM basis.pharmaceutical pellets,Intermidiates ?Our finished formulations from WHO-GMP and EU-GMP units are registered/being registered in 26 countries within Asia, Europe, North America, Latin America and Africa continents including Peru, Panama, Ecuador, Chile, Curaçao, Suriname, Haiti, Aruba, Trinidad, Tobago, Philippines, Myanmar, Laos, Malaysia, Thailand, Indonesia, Hong Kong, Vietnam, Sri Lanka, Maldives, Brunei, Nepal, China, Russia, Croatia, Venezuela and Bhutan.?vishvesh.shaishav@gmail.com
+919725487108
+919726387108
info@eqpharma.com
we offer Oxetacaine API
vikash@sugamts.com
Hi There.
We have earlier supplied Oxetcaine API for exports and can cater to your requirement very well. And the facility is WHOGMP approved. You can write to us with exact requirement, timeline and we will get back within 24 hrs.
Bests.
