IOL Chemicals is an innovation-driven bulk drug, Intermediate and Specialty Chemicals company.
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IOL Chemicals is an innovation-driven bulk drug, Intermediate and Specialty Chemicals company.
Date of Issue : 2022-03-24
Valid Till : 2025-03-17
Written Confirmation Number : WC-0004
Address of the Firm : Village Fatehgarh Chana, Mansa Road, Barnala, Punjab
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Date of Issue : 2022-06-17
Valid Till : 2025-07-07
Written Confirmation Number : WC-0067
Address of the Firm : Chemical Technical Operations Unit-VI, APIIC Industrial Estate, Pydibhimavaram V...
Neuland Laboratories- A dedicated 100% API provider.
Date of Issue : 2022-07-28
Valid Till : 2025-06-16
Written Confirmation Number : WC-0036
Address of the Firm : Unit-1, Sy. No. 347, 473, 474, 490/2, Bonthapally Village, Veerabhadraswamy, Tem...
Neuland Laboratories- A dedicated 100% API provider.
Date of Issue : 2022-06-08
Valid Till : 2025-06-16
Written Confirmation Number : WC-0037
Address of the Firm : Unit-II, Plot No.92-94, 257-259, IDA Pashmylaram, Isnapur Village, Patancheru Ma...
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.
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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.
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A Levetiracetam written confirmation (Levetiracetam WC) is an official document issued by a regulatory agency to a Levetiracetam manufacturer, verifying that the manufacturing facility of a Levetiracetam active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Levetiracetam APIs or Levetiracetam finished pharmaceutical products to another nation, regulatory agencies frequently require a Levetiracetam WC (written confirmation) as part of the regulatory process.
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