01 1BIOTIKA a.s.
02 1Fagron Services B.V.
03 1Hangzhou Zhongmei Huadong Pharmaceutical Co., Ltd
04 1Hangzhou Zhongmei Huadong Pharmaceutical Co., Ltd.
05 1Isomedix Operations Inc
06 2Josun International Limited
07 1LETCO MEDICAL, LLC
08 1Medisca Inc.
09 3North China Pharmaceutical Huasheng Co. Ltd.
10 1Professional Compounding Centers of America dba PCCA
11 1Shandong Haixin Biopharmaceutical, Co. Ltd.
12 1Shandong Luxi Pharmaceutical Co., Ltd.
13 1Spectrum Laboratory Products, Inc.
14 4Xellia Pharmaceuticals ApS
01 2POLYMYXIN B SULFATE
02 16Polymyxin B Sulfate
03 1Polymyxin B Sulphate
04 1Polymyxin B sulfate
01 9China
02 4Denmark
03 1Netherlands
04 1Slovakia
05 4U.S.A
06 1United Kingdom
NDC Package Code : 54563-008
Start Marketing Date : 2010-01-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51551-0304
Start Marketing Date : 2017-02-06
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51551-0306
Start Marketing Date : 2018-03-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-0045
Start Marketing Date : 2015-06-22
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 51927-1086
Start Marketing Date : 2002-07-19
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 49452-5600
Start Marketing Date : 1993-03-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1mg/U)
Marketing Category : DRUG FOR FURTHER PROCESSING
NDC Package Code : 45932-0018
Start Marketing Date : 1998-09-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 45932-0002
Start Marketing Date : 1999-06-10
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 45932-0017
Start Marketing Date : 1999-06-10
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 45932-0001
Start Marketing Date : 1998-09-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Polymyxin B Sulfate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Polymyxin B Sulfate, including repackagers and relabelers. The FDA regulates Polymyxin B Sulfate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Polymyxin B Sulfate 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 Polymyxin B Sulfate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Polymyxin B Sulfate supplier is an individual or a company that provides Polymyxin B Sulfate active pharmaceutical ingredient (API) or Polymyxin B Sulfate finished formulations upon request. The Polymyxin B Sulfate suppliers may include Polymyxin B Sulfate API manufacturers, exporters, distributors and traders.
click here to find a list of Polymyxin B Sulfate 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 Polymyxin B Sulfate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Polymyxin B Sulfate 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 Polymyxin B Sulfate 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 Polymyxin B Sulfate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Polymyxin B Sulfate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Polymyxin B Sulfate suppliers with NDC on PharmaCompass.
We have 13 companies offering Polymyxin B Sulfate
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