Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
01 1M/S Symbiotec Pharmalab
02 1M/s. Symbiotec Pharmalab Ltd
03 1Hubei Gedian Humanwell Pharmaceutical Co., Ltd
01 1Progesterone
02 1Progesterone EP/USP
03 1Progesterone EP/USP, Hydroxy Progesterone Caproate USP
01 1HB230032
02 1WC-0161A2
03 1WC-0162A2
01 1China
02 2India
Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
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
Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
Progesterone EP/USP, Hydroxy Progesterone Caproate 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-...
Date of Issue : 2023-11-13
Valid Till : 2026-11-12
Written Confirmation Number : HB230032
Address of the Firm : No.25, Juxian Road, Cedian Economic Development District, E-zhou City, Hubei, Pr...
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PharmaCompass offers a list of Progesterone 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 Progesterone manufacturer or Progesterone supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Progesterone manufacturer or Progesterone supplier.
PharmaCompass also assists you with knowing the Progesterone API Price utilized in the formulation of products. Progesterone API Price is not always fixed or binding as the Progesterone Price is obtained through a variety of data sources. The Progesterone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Bio-luton manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Bio-luton, including repackagers and relabelers. The FDA regulates Bio-luton manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Bio-luton 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 Bio-luton manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Bio-luton supplier is an individual or a company that provides Bio-luton active pharmaceutical ingredient (API) or Bio-luton finished formulations upon request. The Bio-luton suppliers may include Bio-luton API manufacturers, exporters, distributors and traders.
click here to find a list of Bio-luton suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Bio-luton written confirmation (Bio-luton WC) is an official document issued by a regulatory agency to a Bio-luton manufacturer, verifying that the manufacturing facility of a Bio-luton active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Bio-luton APIs or Bio-luton finished pharmaceutical products to another nation, regulatory agencies frequently require a Bio-luton WC (written confirmation) as part of the regulatory process.
click here to find a list of Bio-luton suppliers with Written Confirmation (WC) on PharmaCompass.
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