Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
01 1M/S Symbiotec Pharmalab
02 2M/s. Symbiotec Pharmalab Ltd
01 1Desogestrel BP/ EP
02 2Desogestrel BP/EP
01 1WC-0161A2
02 2WC-0162A2
01 3India
Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
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
Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
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-...
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
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PharmaCompass offers a list of Desogestrel 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 Desogestrel manufacturer or Desogestrel supplier for your needs.
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PharmaCompass also assists you with knowing the Desogestrel API Price utilized in the formulation of products. Desogestrel API Price is not always fixed or binding as the Desogestrel Price is obtained through a variety of data sources. The Desogestrel Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A VIORELE manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of VIORELE, including repackagers and relabelers. The FDA regulates VIORELE manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. VIORELE 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 VIORELE manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A VIORELE supplier is an individual or a company that provides VIORELE active pharmaceutical ingredient (API) or VIORELE finished formulations upon request. The VIORELE suppliers may include VIORELE API manufacturers, exporters, distributors and traders.
click here to find a list of VIORELE suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A VIORELE written confirmation (VIORELE WC) is an official document issued by a regulatory agency to a VIORELE manufacturer, verifying that the manufacturing facility of a VIORELE active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting VIORELE APIs or VIORELE finished pharmaceutical products to another nation, regulatory agencies frequently require a VIORELE WC (written confirmation) as part of the regulatory process.
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