Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
01 8Pharmaceutical Works POLPHARMA
02 1Supriya Lifescience Limited
03 1Fagron Inc
04 1HIKAL LIMITED
05 1Kalchem International inc
06 1LETCO MEDICAL, LLC
07 1Medisca Inc.
08 1Olon S.p.A.
09 1Professional Compounding Centers of America
10 1Professional Compounding Centers of America dba PCCA
11 1SOLARA ACTIVE PHARMA SCIENCES LIMITED
12 1SUN PHARMACEUTICAL INDUSTRIES, INC.
13 1Spectrum Laboratory Products, Inc.
01 6PENTOXIFYLLINE
02 13Pentoxifylline
03 1Pentoxifyllline
01 4India
02 1Italy
03 1Netherlands
04 8Poland
05 4U.S.A
06 2United Kingdom
Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
NDC Package Code : 12658-0487
Start Marketing Date : 1998-07-20
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
NDC Package Code : 61281-3500
Start Marketing Date : 2016-11-02
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
NDC Package Code : 12658-0618
Start Marketing Date : 1998-07-20
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (24kg/24kg)
Marketing Category : BULK INGREDIENT
Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
NDC Package Code : 12658-0616
Start Marketing Date : 1998-07-20
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (13kg/13kg)
Marketing Category : BULK INGREDIENT
Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
NDC Package Code : 12658-0619
Start Marketing Date : 1998-07-20
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (19kg/19kg)
Marketing Category : BULK INGREDIENT
Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
NDC Package Code : 12658-0617
Start Marketing Date : 1998-07-20
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (21kg/21kg)
Marketing Category : BULK INGREDIENT
Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
NDC Package Code : 12658-0620
Start Marketing Date : 1998-07-20
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (3kg/3kg)
Marketing Category : BULK INGREDIENT
Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
NDC Package Code : 12658-0615
Start Marketing Date : 1998-07-20
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (22kg/22kg)
Marketing Category : BULK INGREDIENT
Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
NDC Package Code : 12658-0515
Start Marketing Date : 1998-07-20
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (10kg/10kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17337-0426
Start Marketing Date : 2017-12-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Pentoxifylline API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Pentoxifylline manufacturer or Pentoxifylline supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Pentoxifylline manufacturer or Pentoxifylline supplier.
PharmaCompass also assists you with knowing the Pentoxifylline API Price utilized in the formulation of products. Pentoxifylline API Price is not always fixed or binding as the Pentoxifylline Price is obtained through a variety of data sources. The Pentoxifylline Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Trental manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Trental, including repackagers and relabelers. The FDA regulates Trental manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Trental 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 Trental manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Trental supplier is an individual or a company that provides Trental active pharmaceutical ingredient (API) or Trental finished formulations upon request. The Trental suppliers may include Trental API manufacturers, exporters, distributors and traders.
click here to find a list of Trental 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 Trental as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Trental 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 Trental 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 Trental and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Trental NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Trental suppliers with NDC on PharmaCompass.
We have 12 companies offering Trental
Get in contact with the supplier of your choice:
