01 1Fujifilm Diosynth Biotechnologies
02 1Lupin Ltd
03 1SIMS Srl
01 16-ALPHA-METHYLPREDNISOLONE SODIUM SUCCINATE
02 1METHYLPREDNISOLONE SOD. SUCCINATE (THIS DMF FORMERLY HELD BY S.I.R.S)
03 1METHYLPREDNISOLONE SODIUM SUCCINATE
01 1India
02 1Italy
03 1United Kingdom
01 1Active
02 2Inactive
01 3Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 6560
Submission : 1986-08-29
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 30375
Submission : 2016-04-15
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 4659
Submission : 1982-08-24
Status : Inactive
Type : II
91
PharmaCompass offers a list of Methylprednisolone Sodium Succinate 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 Sodium Succinate manufacturer or Methylprednisolone Sodium Succinate supplier for your needs.
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A Solumedrol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Solumedrol, including repackagers and relabelers. The FDA regulates Solumedrol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Solumedrol 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 Solumedrol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Solumedrol supplier is an individual or a company that provides Solumedrol active pharmaceutical ingredient (API) or Solumedrol finished formulations upon request. The Solumedrol suppliers may include Solumedrol API manufacturers, exporters, distributors and traders.
click here to find a list of Solumedrol suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Solumedrol DMF (Drug Master File) is a document detailing the whole manufacturing process of Solumedrol active pharmaceutical ingredient (API) in detail. Different forms of Solumedrol DMFs exist exist since differing nations have different regulations, such as Solumedrol USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Solumedrol DMF submitted to regulatory agencies in the US is known as a USDMF. Solumedrol USDMF includes data on Solumedrol's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Solumedrol USDMF is kept confidential to protect the manufacturer’s intellectual property.
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