Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
01 1M/S Symbiotec Pharmalab
02 2M/s. Symbiotec Pharmalab Ltd
03 1M/s. Avik Pharmaceutical Limited
Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
Methyl Prednisolone Acetate USP, Methyl Prednisolone 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
Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
Methyl Prednisolone 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-...
Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
Methyl prednisolone acetate USP/Methyl PrednisoloneBP/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 Methylprednisolone 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 Methylprednisolone Acetate manufacturer or Methylprednisolone Acetate supplier for your needs.
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PharmaCompass also assists you with knowing the Methylprednisolone Acetate API Price utilized in the formulation of products. Methylprednisolone Acetate API Price is not always fixed or binding as the Methylprednisolone Acetate Price is obtained through a variety of data sources. The Methylprednisolone Acetate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Depo-Medrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Depo-Medrate, including repackagers and relabelers. The FDA regulates Depo-Medrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Depo-Medrate 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 Depo-Medrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Depo-Medrate supplier is an individual or a company that provides Depo-Medrate active pharmaceutical ingredient (API) or Depo-Medrate finished formulations upon request. The Depo-Medrate suppliers may include Depo-Medrate API manufacturers, exporters, distributors and traders.
click here to find a list of Depo-Medrate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Depo-Medrate written confirmation (Depo-Medrate WC) is an official document issued by a regulatory agency to a Depo-Medrate manufacturer, verifying that the manufacturing facility of a Depo-Medrate active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Depo-Medrate APIs or Depo-Medrate finished pharmaceutical products to another nation, regulatory agencies frequently require a Depo-Medrate WC (written confirmation) as part of the regulatory process.
click here to find a list of Depo-Medrate suppliers with Written Confirmation (WC) on PharmaCompass.
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