Neuland Laboratories- A dedicated 100% API provider.

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01 1M/s Neuland Laboratories Ltd
02 1M/sShodhana laboratories limited
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01 2Rotigotine IH
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01 1WC-0036
02 1WC-0230
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01 2India
Date of Issue : 2025-06-16
Valid Till : 2028-06-16
Written Confirmation Number : WC-0036
Address of the Firm : (Unit-l), Sy.No.291, 346P, 347, 348P, 473, 474, 490/2, Veerabhadraswamy Temple R...
Date of Issue : 2025-10-17
Valid Till : 2028-07-07
Written Confirmation Number : WC-0230
Address of the Firm : Plot No.24, 25 & 26, Phase-I, IDA, Jeedimetla, Medchai District-500 055, Telanga...

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PharmaCompass offers a list of Rotigotine API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Rotigotine manufacturer or Rotigotine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Rotigotine manufacturer or Rotigotine supplier.
A Leganto manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Leganto, including repackagers and relabelers. The FDA regulates Leganto manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Leganto 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 Leganto manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Leganto supplier is an individual or a company that provides Leganto active pharmaceutical ingredient (API) or Leganto finished formulations upon request. The Leganto suppliers may include Leganto API manufacturers, exporters, distributors and traders.
click here to find a list of Leganto suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Leganto written confirmation (Leganto WC) is an official document issued by a regulatory agency to a Leganto manufacturer, verifying that the manufacturing facility of a Leganto active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Leganto APIs or Leganto finished pharmaceutical products to another nation, regulatory agencies frequently require a Leganto WC (written confirmation) as part of the regulatory process.
click here to find a list of Leganto suppliers with Written Confirmation (WC) on PharmaCompass.
We have 2 companies offering Leganto
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