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01 12Pharmaceutical 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.

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothPolpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.

PENTOXIFYLLINE

NDC Package Code : 12658-0434

Start Marketing Date : 1998-07-20

End Marketing Date : 2024-12-31

Dosage Form (Strength) : POWDER (25kg/25kg)

Marketing Category : BULK INGREDIENT

Polpharma CB

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSupriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.

PENTOXIFYLLINE

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

Supriya

03

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothPolpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.

PENTOXIFYLLINE

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

Polpharma CB

04

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothPolpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.

PENTOXIFYLLINE

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

Polpharma CB

05

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothPolpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.

PENTOXIFYLLINE

NDC Package Code : 12658-0507

Start Marketing Date : 1998-07-20

End Marketing Date : 2024-12-31

Dosage Form (Strength) : POWDER (30kg/30kg)

Marketing Category : BULK INGREDIENT

Polpharma CB

06

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothPolpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.

PENTOXIFYLLINE

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 CB

07

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothPolpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.

PENTOXIFYLLINE

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 CB

08

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothPolpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.

PENTOXIFYLLINE

NDC Package Code : 12658-0610

Start Marketing Date : 1998-07-20

End Marketing Date : 2024-12-31

Dosage Form (Strength) : POWDER (17kg/17kg)

Marketing Category : BULK INGREDIENT

Polpharma CB

09

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothPolpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.

PENTOXIFYLLINE

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 CB

10

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothPolpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.

PENTOXIFYLLINE

NDC Package Code : 12658-0611

Start Marketing Date : 1998-07-20

End Marketing Date : 2024-12-31

Dosage Form (Strength) : POWDER (23kg/23kg)

Marketing Category : BULK INGREDIENT

Polpharma CB

Pentoxifylline Manufacturers

A Pentoxifylline manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Pentoxifylline, including repackagers and relabelers. The FDA regulates Pentoxifylline manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Pentoxifylline 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 Pentoxifylline manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

Pentoxifylline Suppliers

A Pentoxifylline supplier is an individual or a company that provides Pentoxifylline active pharmaceutical ingredient (API) or Pentoxifylline finished formulations upon request. The Pentoxifylline suppliers may include Pentoxifylline API manufacturers, exporters, distributors and traders.

click here to find a list of Pentoxifylline suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

Pentoxifylline NDC

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 Pentoxifylline as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for Pentoxifylline API and other APIs are published in this directory by the FDA.

Unfinished drugs

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 Pentoxifylline 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.

Compounded drug products

The NDC directory also contains data on finished compounded human drug products that contain Pentoxifylline and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Pentoxifylline NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of Pentoxifylline suppliers with NDC on PharmaCompass.

Pentoxifylline Manufacturers | Traders | Suppliers

Pentoxifylline Manufacturers, Traders, Suppliers 1
Inform the supplier about your product requirements, specifying if you need a product with particular monograph like EP (Ph. Eur.), USP, JP, BP, or any other quality. In addition, clarify whether you need hydrochloride (HCl), anhydricum, base, micronisatum or a specific level of purity. To find reputable suppliers, utilize the filters and select those certified by GMP, FDA, or any other certification as per your requirement.
For your convenience, we have listed synonyms and CAS numbers to help you find the best supplier. The use of synonyms and CAS numbers can be helpful in identifying potential suppliers, but it is crucial to note that they might not always indicate the exact same product. It is important to confirm the product details with the supplier before making a purchase to ensure that it meets your requirements.