DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 3Dr. Reddy's Laboratories
02 1Alembic Pharmaceuticals Limited
03 1Biocon
04 2MSN Laboratories
05 1Natco Pharma
06 2Sichuan Elixir Pharmaceuticals
07 1Sun Pharmaceutical Industries Limited
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 38207
Submission : 2023-03-31
Status :
Type : II
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 39141
Submission : 2023-12-01
Status :
Type : II
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 39274
Submission : 2023-12-29
Status :
Type : II
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PharmaCompass offers a list of Cabozantinib S-Malate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Cabozantinib S-Malate manufacturer or Cabozantinib S-Malate supplier for your needs.
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A CABOMETYX manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CABOMETYX, including repackagers and relabelers. The FDA regulates CABOMETYX manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CABOMETYX API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A CABOMETYX supplier is an individual or a company that provides CABOMETYX active pharmaceutical ingredient (API) or CABOMETYX finished formulations upon request. The CABOMETYX suppliers may include CABOMETYX API manufacturers, exporters, distributors and traders.
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A CABOMETYX DMF (Drug Master File) is a document detailing the whole manufacturing process of CABOMETYX active pharmaceutical ingredient (API) in detail. Different forms of CABOMETYX DMFs exist exist since differing nations have different regulations, such as CABOMETYX USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A CABOMETYX DMF submitted to regulatory agencies in the US is known as a USDMF. CABOMETYX USDMF includes data on CABOMETYX's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The CABOMETYX USDMF is kept confidential to protect the manufacturer’s intellectual property.
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