DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 1Dr. Reddy's Laboratories Ltd.
02 1Neuland Laboratories Limited.
03 1Apitoria Pharma Private Limited
04 1DIVI'S LABORATORIES LIMITED
05 2Hetero Labs Limited
06 1LUPIN LIMITED.
07 1Solara Active Pharma Sciences Limited
08 2Zhejiang Huahai Pharmaceutical Co. , Ltd.
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Registration Number : 302MF10034
Registrant's Address : 8-2-337, Road No. 3, Banjara Hills, Hyderabad 500 034, TELANGANA, INDIA
Initial Date of Registration : 2020-03-09
Latest Date of Registration : 2020-03-09
Neuland Laboratories- A dedicated 100% API provider.
Registration Number : 302MF10084
Registrant's Address : 11th Floor (5th Office Level), Phoenix IVV Building, Plot No. 573A-Ⅲ, Road No. 82, ...
Initial Date of Registration : 2020-07-16
Latest Date of Registration : 2020-07-16
A Levetiracetam manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Levetiracetam, including repackagers and relabelers. The FDA regulates Levetiracetam manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Levetiracetam API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Levetiracetam manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Levetiracetam supplier is an individual or a company that provides Levetiracetam active pharmaceutical ingredient (API) or Levetiracetam finished formulations upon request. The Levetiracetam suppliers may include Levetiracetam API manufacturers, exporters, distributors and traders.
click here to find a list of Levetiracetam suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Levetiracetam Drug Master File in Japan (Levetiracetam JDMF) empowers Levetiracetam API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Levetiracetam JDMF during the approval evaluation for pharmaceutical products. At the time of Levetiracetam JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Levetiracetam suppliers with JDMF on PharmaCompass.
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