Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
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01 1M/S Symbiotec Pharmalab
02 2M/s. Symbiotec Pharmalab Ltd
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01 1Hydrocortisone Acetate (BP/EP/USP)
02 1Hydrocortisone Acetate BP/EP/USP
03 1Hydrocortisone AcetateBP/EP/USP
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01 1WC-0161A2
02 2WC-0162A2
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01 3India
Hydrocortisone Acetate BP/EP/USP
Date of Issue : 2022-09-30
Valid Till : 2025-07-02
Written Confirmation Number : WC-0162A2
Address of the Firm : 385/2, Pigdamber, Rau, Indore-453 331, MP, India
Hydrocortisone Acetate (BP/EP/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 AcetateBP/EP/USP
Date of Issue : 2022-07-05
Valid Till : 2025-07-02
Written Confirmation Number : WC-0161A2
Address of the Firm : 385/2, Pigdamber, Rau, Indore-453 331, MP, India
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PharmaCompass offers a list of Hydrocortisone Acetate 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 Hydrocortisone Acetate manufacturer or Hydrocortisone Acetate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Hydrocortisone Acetate manufacturer or Hydrocortisone Acetate supplier.
PharmaCompass also assists you with knowing the Hydrocortisone Acetate API Price utilized in the formulation of products. Hydrocortisone Acetate API Price is not always fixed or binding as the Hydrocortisone Acetate Price is obtained through a variety of data sources. The Hydrocortisone Acetate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A U-CORT manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of U-CORT, including repackagers and relabelers. The FDA regulates U-CORT manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. U-CORT 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 U-CORT manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A U-CORT supplier is an individual or a company that provides U-CORT active pharmaceutical ingredient (API) or U-CORT finished formulations upon request. The U-CORT suppliers may include U-CORT API manufacturers, exporters, distributors and traders.
click here to find a list of U-CORT suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A U-CORT written confirmation (U-CORT WC) is an official document issued by a regulatory agency to a U-CORT manufacturer, verifying that the manufacturing facility of a U-CORT active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting U-CORT APIs or U-CORT finished pharmaceutical products to another nation, regulatory agencies frequently require a U-CORT WC (written confirmation) as part of the regulatory process.
click here to find a list of U-CORT suppliers with Written Confirmation (WC) on PharmaCompass.
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