01 1M/s Symed Labs Limited
02 1Shilpa Pharma Lifesciences
01 1Thalidomide IH/USP
02 1Thalidomide USP
01 1WC-0072
02 1WC-0148
01 2India
Date of Issue : 2025-10-09
Valid Till : 2028-07-02
Written Confirmation Number : WC-0148
Address of the Firm : 1A & 1A \'P\', 1B, 2, 2A, 2B, 3A to 3E, 4A, 5A, 4B & 5B, Deosugur Industrial Are...
Date of Issue : 2025-09-29
Valid Till : 2028-08-09
Written Confirmation Number : WC-0072
Address of the Firm : Unit-II, Plot No.: 25/B, Phase -III, Jeedimetla(V),Quthbullapur (M), Medchal -Ma...
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A Glutarimide, 2-phthalimido- manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Glutarimide, 2-phthalimido-, including repackagers and relabelers. The FDA regulates Glutarimide, 2-phthalimido- manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Glutarimide, 2-phthalimido- 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 Glutarimide, 2-phthalimido- manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Glutarimide, 2-phthalimido- supplier is an individual or a company that provides Glutarimide, 2-phthalimido- active pharmaceutical ingredient (API) or Glutarimide, 2-phthalimido- finished formulations upon request. The Glutarimide, 2-phthalimido- suppliers may include Glutarimide, 2-phthalimido- API manufacturers, exporters, distributors and traders.
click here to find a list of Glutarimide, 2-phthalimido- suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Glutarimide, 2-phthalimido- written confirmation (Glutarimide, 2-phthalimido- WC) is an official document issued by a regulatory agency to a Glutarimide, 2-phthalimido- manufacturer, verifying that the manufacturing facility of a Glutarimide, 2-phthalimido- active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Glutarimide, 2-phthalimido- APIs or Glutarimide, 2-phthalimido- finished pharmaceutical products to another nation, regulatory agencies frequently require a Glutarimide, 2-phthalimido- WC (written confirmation) as part of the regulatory process.
click here to find a list of Glutarimide, 2-phthalimido- suppliers with Written Confirmation (WC) on PharmaCompass.
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