Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
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01 1M/s. Symbiotec Pharmalab Ltd
02 1M/s. Mac-Chem Products (India) Pvt. Ltd
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01 1HYDROCORTISONE SODIUM SUCCINATE
02 1Hydrocortisone Hemisuccinate (BP/USP)
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01 1WC-0162A2
02 1WC-0275
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01 2India
Hydrocortisone Hemisuccinate (BP/USP)
Date of Issue : 2022-08-31
Valid Till : 2025-07-02
Written Confirmation Number : WC-0162A2
Address of the Firm : Plot No. 5, 6, 7 & 8 Special Economic Zone, Phase II, Pithampur, Dist: Dhar, MP-...
HYDROCORTISONE SODIUM SUCCINATE
Date of Issue : 2021-01-22
Valid Till : 2023-08-01
Written Confirmation Number : WC-0275
Address of the Firm : N-211/2/10, MIDC, Boisar, Dist-Thane-401506, Mahrashtra
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PharmaCompass also assists you with knowing the Hydrocortisone Sodium Succinate API Price utilized in the formulation of products. Hydrocortisone Sodium Succinate API Price is not always fixed or binding as the Hydrocortisone Sodium Succinate Price is obtained through a variety of data sources. The Hydrocortisone Sodium Succinate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Sopolkort manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sopolkort, including repackagers and relabelers. The FDA regulates Sopolkort manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sopolkort 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 Sopolkort supplier is an individual or a company that provides Sopolkort active pharmaceutical ingredient (API) or Sopolkort finished formulations upon request. The Sopolkort suppliers may include Sopolkort API manufacturers, exporters, distributors and traders.
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A Sopolkort written confirmation (Sopolkort WC) is an official document issued by a regulatory agency to a Sopolkort manufacturer, verifying that the manufacturing facility of a Sopolkort active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Sopolkort APIs or Sopolkort finished pharmaceutical products to another nation, regulatory agencies frequently require a Sopolkort WC (written confirmation) as part of the regulatory process.
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