Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.

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01 1M/s Symbiotec Pharmalab Private limited
02 2M/s Symbiotec Pharmalab Pvt Ltd
03 1SYMBIOTICA SPECIALITY INGREDIENTS SDN. BHD.
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01 2Methyl Prednisolone Acetate USP
02 1Methylprednisolone Acetate
03 1Methylprednisolone Acetate BP/EP/USP
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01 13923/25
02 1WC-0161A2
03 1WC-0161n
04 1WC-0162n
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01 3India
02 1Malaysia
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
Symbiotica delivers high-quality APIs through advanced R&D, GMP-certified manufacturing, & trusted global pharmaceutical partnerships.
Date of Issue : 2025-05-20
Valid Till : 2028-05-22
Written Confirmation Number : 3923/25
Address of the Firm : No. 518, Jalan Waja 4, Taman Industri Waja, 09000 Kulim, Kedah, Malaysia
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
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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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, and COA 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, and COA 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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