Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
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01 1M/s Symbiotec Pharmalab Private Limited
02 1M/s Symbiotec Pharmalab Private limited
03 2M/s Symbiotec Pharmalab Pvt Ltd
04 1M/s Symbiotec Pharmalab Pvt ltd
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01 2Methyl Prednisolone Acetate USP
02 2Methylprednisolone Acetate BP/EP/USP
03 1Methylprednisolone Acetate USP
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01 1WC-0161A
02 1WC-0161A2
03 1WC-0161n
04 1WC-0162A2
05 1WC-0162n
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01 5India
Methylprednisolone Acetate BP/EP/USP
Date of Issue : 2022-06-30
Valid Till : 2025-07-02
Written Confirmation Number : WC-0161A
Address of the Firm : 385/2, Gram Pigdamber, Rau , Indore-453331, Madhya Pradesh, India
Methyl Prednisolone Acetate USP
Date of Issue : 2022-06-30
Valid Till : 2025-07-02
Written Confirmation Number : WC-0161A2
Address of the Firm : 385/2, Gram Pigdamber, Rau, Indore-453331, M.P., India
Methylprednisolone Acetate BP/EP/USP
Date of Issue : 2022-06-30
Valid Till : 2025-07-02
Written Confirmation Number : WC-0161n
Address of the Firm : PLOT NO.385/2, Gram Pigdamber, Rau , Indore-453331, Madhya Pradesh, India
Methylprednisolone Acetate USP
Date of Issue : 2022-08-31
Valid Till : 2025-02-07
Written Confirmation Number : WC-0162A2
Address of the Firm : Plot No. 5,6,7 &8, Special Economic Zone, Phase II, Pharma Zone, Pithampur, Dist...
Methyl Prednisolone Acetate USP
Date of Issue : 2022-07-23
Valid Till : 2025-02-07
Written Confirmation Number : WC-0162n
Address of the Firm : Plot No-5,6,7 & 8, Special Economic Zone, Phase-II, Pharma Zone, Pithampur, Dist...
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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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