Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
01 1M/s Supriya Lifesience Ltd
02 1M/s Melody Healthcare Pvt Ltd
03 1M/s. Cipla Ltd
01 2Levosalbutamol Sulphate IH
02 1Levosalbutamol Sulphate IP/IH
01 1WC-0142n
02 1WC-0218
03 1WC-0227n
01 3India
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
Date of Issue : 2022-06-29
Valid Till : 2025-07-02
Written Confirmation Number : WC-0218
Address of the Firm : A-5/2, Late Parshuram Industrial Area, MIDC, Tal-Khed, Dist. Ratnagiri-415 722, ...
Date of Issue : 2022-06-17
Valid Till : 2025-08-04
Written Confirmation Number : WC-0142n
Address of the Firm : Plot. A-33, A-37/2/2 MIDC, Patalganga-410 220, Dist. Raigad, Maharashtra
Date of Issue : 2022-07-28
Valid Till : 2025-07-02
Written Confirmation Number : WC-0227n
Address of the Firm : Plot No. J-73, MIDC, Tarapur, Boisar, Dist- Palghar 401506, Maharashtra, India
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PharmaCompass offers a list of Levalbuterol Sulfate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Levalbuterol Sulfate manufacturer or Levalbuterol Sulfate supplier for your needs.
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PharmaCompass also assists you with knowing the Levalbuterol Sulfate API Price utilized in the formulation of products. Levalbuterol Sulfate API Price is not always fixed or binding as the Levalbuterol Sulfate Price is obtained through a variety of data sources. The Levalbuterol Sulfate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Levosalbutamol Sulphate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Levosalbutamol Sulphate, including repackagers and relabelers. The FDA regulates Levosalbutamol Sulphate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Levosalbutamol Sulphate 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 Levosalbutamol Sulphate supplier is an individual or a company that provides Levosalbutamol Sulphate active pharmaceutical ingredient (API) or Levosalbutamol Sulphate finished formulations upon request. The Levosalbutamol Sulphate suppliers may include Levosalbutamol Sulphate API manufacturers, exporters, distributors and traders.
click here to find a list of Levosalbutamol Sulphate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Levosalbutamol Sulphate written confirmation (Levosalbutamol Sulphate WC) is an official document issued by a regulatory agency to a Levosalbutamol Sulphate manufacturer, verifying that the manufacturing facility of a Levosalbutamol Sulphate active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Levosalbutamol Sulphate APIs or Levosalbutamol Sulphate finished pharmaceutical products to another nation, regulatory agencies frequently require a Levosalbutamol Sulphate WC (written confirmation) as part of the regulatory process.
click here to find a list of Levosalbutamol Sulphate suppliers with Written Confirmation (WC) on PharmaCompass.
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