Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
01 1Symbiotec Pharmalab Private Limited
02 2Farmabios S.p.A.
03 2EUROAPI FRANCE
04 1Henan Lihua Pharmaceutical Co Ltd
05 1Medisca Inc.
06 1SYMBIOTICA SPECIALITY INGREDIENTS SDN.BHD
07 1Spectrum Laboratory Products, Inc.
08 1zhejiang xianju pharmaceutical co., Ltd.
01 3PREDNISOLONE ACETATE
02 4Prednisolone Acetate
03 2Prednisolone acetate
04 1prednisolone acetate
01 2China
02 2France
03 2Germany
04 1India
05 1Malaysia
06 2U.S.A
Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
NDC Package Code : 22552-0044
Start Marketing Date : 2015-10-26
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 : 46439-8761
Start Marketing Date : 2018-05-31
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 : 82298-107
Start Marketing Date : 2011-02-07
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Axplora- The partner of choice for complex APIs.
NDC Package Code : 46439-8776
Start Marketing Date : 2024-09-23
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 : 82298-108
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 : 64958-0048
Start Marketing Date : 2003-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-0152
Start Marketing Date : 2014-06-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49452-5990
Start Marketing Date : 1992-11-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 52128-150
Start Marketing Date : 2010-11-25
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 60722-3006
Start Marketing Date : 2020-10-23
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Prednisolone Acetate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Prednisolone Acetate, including repackagers and relabelers. The FDA regulates Prednisolone Acetate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Prednisolone 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 Prednisolone Acetate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Prednisolone Acetate supplier is an individual or a company that provides Prednisolone Acetate active pharmaceutical ingredient (API) or Prednisolone Acetate finished formulations upon request. The Prednisolone Acetate suppliers may include Prednisolone Acetate API manufacturers, exporters, distributors and traders.
click here to find a list of Prednisolone 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 Prednisolone Acetate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Prednisolone 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 Prednisolone 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 Prednisolone Acetate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Prednisolone Acetate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Prednisolone Acetate suppliers with NDC on PharmaCompass.
We have 8 companies offering Prednisolone Acetate
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?
