01 1Apicore Pharmaceuticals Private Limited
02 1Aragen Life Sciences Limited
03 1Darmerica, LLC
04 2Indena SpA
05 1Kalchem International inc
06 1LETCO MEDICAL, LLC
07 1MOLCLONE LABS PRIVATE LIMITED
08 1Medisca Inc.
09 1Micro Labs Limited
10 1Professional Compounding Centers of America dba PCCA
11 1Sentio Biosciences, LLC
12 2Swati Spentose Private Limited
13 1bene pharmaChem GmbH & Co. KG
01 6PENTOSAN POLYSULFATE SODIUM
02 8Pentosan Polysulfate Sodium
03 1Pentosan Polysulfte Sodium
01 1Germany
02 6India
03 2Italy
04 5U.S.A
05 1United Kingdom
NDC Package Code : 42973-118
Start Marketing Date : 2009-11-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 29967-0001
Start Marketing Date : 2009-07-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 42897-001
Start Marketing Date : 1996-11-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17359-3800
Start Marketing Date : 2021-05-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17359-3805
Start Marketing Date : 2023-12-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-2706
Start Marketing Date : 2013-03-08
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 42571-476
Start Marketing Date : 2024-07-22
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (10kg/10kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-0052
Start Marketing Date : 2018-10-23
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 49405-000
Start Marketing Date : 2011-04-07
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (20kg/20kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 52119-005
Start Marketing Date : 2012-08-20
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Sodium, Pentosan Polysulphate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sodium, Pentosan Polysulphate, including repackagers and relabelers. The FDA regulates Sodium, Pentosan Polysulphate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sodium, Pentosan Polysulphate 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 Sodium, Pentosan Polysulphate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sodium, Pentosan Polysulphate supplier is an individual or a company that provides Sodium, Pentosan Polysulphate active pharmaceutical ingredient (API) or Sodium, Pentosan Polysulphate finished formulations upon request. The Sodium, Pentosan Polysulphate suppliers may include Sodium, Pentosan Polysulphate API manufacturers, exporters, distributors and traders.
click here to find a list of Sodium, Pentosan Polysulphate 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 Sodium, Pentosan Polysulphate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Sodium, Pentosan Polysulphate 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 Sodium, Pentosan Polysulphate 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 Sodium, Pentosan Polysulphate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Sodium, Pentosan Polysulphate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Sodium, Pentosan Polysulphate suppliers with NDC on PharmaCompass.
We have 13 companies offering Sodium, Pentosan Polysulphate
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