Symbiotica delivers high-quality APIs through advanced R&D, GMP-certified manufacturing, & trusted global pharmaceutical partnerships.
01 1SYMBIOTICA SPECIALITY INGREDIENTS SDN. BHD.
02 1M/sAvik Pharmaceuticals Limited
01 1Methylprednisolone Aceponate
02 1Methylprednisolone Aceponate IH
01 13923/25
02 1WC-0169
01 1India
02 1Malaysia
Symbiotica delivers high-quality APIs through advanced R&D, GMP-certified manufacturing, & trusted global pharmaceutical partnerships.
Date of Issue : 2025-05-20
Valid Till : 2028-05-22
Written Confirmation Number : 3923/25
Address of the Firm : No. 518, Jalan Waja 4, Taman Industri Waja, 09000 Kulim, Kedah, Malaysia
Methylprednisolone Aceponate IH
Date of Issue : 2024-09-24
Valid Till : 2028-07-02
Written Confirmation Number : WC-0169
Address of the Firm : Plot No. -A-1/7 & A-1/8, 1st Phase, G.I.D.C. Vapі, Dist. -Valsad -396195, Gujar...
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A Lexxema manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lexxema, including repackagers and relabelers. The FDA regulates Lexxema manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lexxema 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 Lexxema manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Lexxema supplier is an individual or a company that provides Lexxema active pharmaceutical ingredient (API) or Lexxema finished formulations upon request. The Lexxema suppliers may include Lexxema API manufacturers, exporters, distributors and traders.
click here to find a list of Lexxema suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Lexxema written confirmation (Lexxema WC) is an official document issued by a regulatory agency to a Lexxema manufacturer, verifying that the manufacturing facility of a Lexxema active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Lexxema APIs or Lexxema finished pharmaceutical products to another nation, regulatory agencies frequently require a Lexxema WC (written confirmation) as part of the regulatory process.
click here to find a list of Lexxema suppliers with Written Confirmation (WC) on PharmaCompass.
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