Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
01 1Symbiotec Pharmalab Private limited
02 1Farmabios S.p.A.
03 1EUROAPI FRANCE
04 1B&B Pharmaceuticals, Inc.
05 1Curia Spain S.A.U.
06 1Curia Spain, S.A.U.
07 1DARMERICA, LLC
08 1Fagron Inc
09 1LETCO MEDICAL, LLC
10 1Medisca Inc.
11 1NEWCHEM SPA
12 1Pharmacia and Upjohn Company LLC
13 1Professional Compounding Centers of America dba PCCA
14 1Sotera Health
15 4Symbiotica Speciality Ingredients Sdn. Bhd.
16 1Willow Birch Pharma, Inc.
17 1Zhejiang Xianju Pharmaceutical Co., Ltd.
01 1METHYLPREDNISOLONE ACETATE
02 11Methylprednisolone Acetate
03 1Methylprednisolone Acetate -Micronized
04 1Methylprednisolone Acetate Micronized
05 4Methylprednisolone acetate
06 1Methylprednisolone acetate sterile
07 1Prednisolone Hemisuccinate
01 1China
02 1France
03 1Germany
04 1India
05 1Italy
06 4Malaysia
07 1Netherlands
08 9U.S.A
09 1United Kingdom
Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
NDC Package Code : 22552-0023
Start Marketing Date : 2011-08-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
Axplora- The partner of choice for complex APIs.
NDC Package Code : 46439-8767
Start Marketing Date : 2018-11-15
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
NDC Package Code : 82298-117
Start Marketing Date : 2011-02-07
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51552-0958
Start Marketing Date : 2004-09-01
End Marketing Date : 2027-04-30
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 38779-0144
Start Marketing Date : 2006-08-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 24002-0010
Start Marketing Date : 2009-08-11
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-0000
Start Marketing Date : 2012-01-20
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 0009-0026
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 : 52128-148
Start Marketing Date : 2012-12-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (5kg/5kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 10695-041
Start Marketing Date : 2017-08-10
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Methylprednisolone Acetate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Methylprednisolone Acetate, including repackagers and relabelers. The FDA regulates Methylprednisolone Acetate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Methylprednisolone Acetate 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 Acetate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Methylprednisolone Acetate supplier is an individual or a company that provides Methylprednisolone Acetate active pharmaceutical ingredient (API) or Methylprednisolone Acetate finished formulations upon request. The Methylprednisolone Acetate suppliers may include Methylprednisolone Acetate API manufacturers, exporters, distributors and traders.
click here to find a list of Methylprednisolone Acetate 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 Acetate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Methylprednisolone Acetate 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 Acetate 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 Acetate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Methylprednisolone Acetate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Methylprednisolone Acetate suppliers with NDC on PharmaCompass.
We have 16 companies offering Methylprednisolone Acetate
Get in contact with the supplier of your choice:
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