Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
01 1Symbiotec Pharmalab Private Limited
02 1EUROAPI FRANCE
03 1Curia Spain S.A.U.
04 1HENAN LIHUA PHARMACEUTICAL CO., LTD.
05 1Pharmacia and Upjohn Company LLC
06 1Professional Compounding Centers of America
07 1STERLING SPA
08 1Spectrum Laboratory Products, Inc.
09 1Tianjin Tianyao Pharmaceuticals Co., Ltd.
10 1Zhejiang Xianju Pharmaceutical Co., Ltd.
01 2METHYLPREDNISOLONE
02 1METHYLPREDNISOLONE SODIUM SULEPTANATE
03 1METHYLPREDNISOLONE SULEPTANATE
04 6Methylprednisolone
01 3China
02 1France
03 1India
04 1Italy
05 3U.S.A
06 1United Kingdom
Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
NDC Package Code : 22552-0029
Start Marketing Date : 2011-08-24
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
NDC Package Code : 82298-118
Start Marketing Date : 2011-02-07
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
METHYLPREDNISOLONE SULEPTANATE
NDC Package Code : 65089-0062
Start Marketing Date : 1979-03-14
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 64958-0084
Start Marketing Date : 1983-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-0201
Start Marketing Date : 2012-08-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 0009-0038
Start Marketing Date : 2014-07-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49452-4686
Start Marketing Date : 1994-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
METHYLPREDNISOLONE SULEPTANATE
NDC Package Code : 64918-1917
Start Marketing Date : 2022-01-04
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 57582-011
Start Marketing Date : 2015-07-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : DRUG FOR FURTHER PROCESSING
NDC Package Code : 60722-1003
Start Marketing Date : 2016-01-06
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Methylprednisolone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Methylprednisolone, including repackagers and relabelers. The FDA regulates Methylprednisolone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Methylprednisolone 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 Methylprednisolone manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Methylprednisolone supplier is an individual or a company that provides Methylprednisolone active pharmaceutical ingredient (API) or Methylprednisolone finished formulations upon request. The Methylprednisolone suppliers may include Methylprednisolone API manufacturers, exporters, distributors and traders.
click here to find a list of Methylprednisolone suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Methylprednisolone as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Methylprednisolone API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture Methylprednisolone as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain Methylprednisolone and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Methylprednisolone NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Methylprednisolone suppliers with NDC on PharmaCompass.
We have 10 companies offering Methylprednisolone
Get in contact with the supplier of your choice:
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