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01 2Minakem Dunkerque Production

02 1VAMSI LABS LIMITED.

03 1Coral Drugs Private Limited

04 2Farmabios S.p.A.

05 1Aspen Oss B.V.

06 1Aarti Pharmalabs Limited

07 1AX Pharmaceutical Corp

08 1Amphastar Nanjing Pharmaceuticals, Inc.

09 2AstraZeneca AB

10 1Cipla Ltd.

11 2Curia Spain, S.A.U.

12 1Darmerica, LLC

13 1Hubei Gedian Humanwell Pharmaceutical Co., Ltd

14 1Hubei Gedian humanwell Pharmaceutical Co., Ltd

15 3Industriale Chimica s.r.l.

16 1KALCHEM INTERNATIONAL INC

17 1LETCO MEDICAL, LLC

18 1Medisca Inc.

19 1NEWCHEM SPA

20 1Professional Compounding Centers of America dba PCCA

21 1SHAKTI LIFESCIENCE PRIVATE LTD

22 1Sicor S.p.a.

23 2Sicor S.r.l.

24 1Sicor de Mexico S.A. de C.V

25 1Spectrum Laboratory Products, Inc.

26 2Sterling S.p.A.

27 1Symbiotica Speciality Ingredients Sdn. Bhd.

28 1Xenex Laboratories Inc

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothMinakem delivers API, HPAPI, steroids & CDMO services for generics with FDA/GMP certification, regulatory know-how & proven success.

BUDESONIDE

NDC Package Code : 49927-0003

Start Marketing Date : 2006-02-05

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (1kg/kg)

Marketing Category : BULK INGREDIENT

Minakem Comapny Banner

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothVamsi Labs is one of the major manufacturers of Anti-asthmatic, Anti-migraine & Anti-psychotic APIs.

BUDESONIDE

NDC Package Code : 66412-0393

Start Marketing Date : 2021-01-05

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (1kg/kg)

Marketing Category : BULK INGREDIENT FOR HUMAN P...

Vamsi Labs

03

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Biotech Showcase
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothCoral's API range includes Corticosteroids, Antihistamines. Hormones and Antineoplastics.

BUDESONIDE

NDC Package Code : 49076-6111

Start Marketing Date : 2017-11-02

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (1kg/kg)

Marketing Category : BULK INGREDIENT

Corel Drugs cGMP partner for APIs

04

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Biotech Showcase
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothAxplora- The partner of choice for complex APIs.

BUDESONIDE

NDC Package Code : 46439-8719

Start Marketing Date : 2005-06-01

End Marketing Date : 2024-12-31

Dosage Form (Strength) : POWDER (1g/g)

Marketing Category : BULK INGREDIENT

Axplora CB

05

BUDESONIDE

NDC Package Code : 60870-0466

Start Marketing Date : 1993-09-23

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (1g/g)

Marketing Category : BULK INGREDIENT

Aspen API Comapny Banner

06

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Biotech Showcase
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothAarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.

BUDESONIDE

NDC Package Code : 15308-0100

Start Marketing Date : 2001-01-01

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (1kg/kg)

Marketing Category : BULK INGREDIENT

Aarti Industries Company Banner

07

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothMinakem delivers API, HPAPI, steroids & CDMO services for generics with FDA/GMP certification, regulatory know-how & proven success.

BUDESONIDE

NDC Package Code : 49927-0004

Start Marketing Date : 2006-02-16

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (1kg/kg)

Marketing Category : BULK INGREDIENT

Minakem Comapny Banner

08

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Biotech Showcase
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothAxplora- The partner of choice for complex APIs.

BUDESONIDE

NDC Package Code : 46439-8737

Start Marketing Date : 2011-04-26

End Marketing Date : 2024-12-31

Dosage Form (Strength) : POWDER (1g/g)

Marketing Category : BULK INGREDIENT

Axplora CB

09

Biotech Showcase
Not Confirmed
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Biotech Showcase
Not Confirmed

BUDESONIDE

NDC Package Code : 17228-1991

Start Marketing Date : 2005-04-01

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (3.4kg/3.4kg)

Marketing Category : BULK INGREDIENT

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10

Biotech Showcase
Not Confirmed
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Biotech Showcase
Not Confirmed

BUDESONIDE

NDC Package Code : 17228-9700

Start Marketing Date : 2023-03-09

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (6kg/6kg)

Marketing Category : BULK INGREDIENT

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Budesonide Manufacturers

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

Budesonide Suppliers

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

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

Budesonide 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 Budesonide as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for Budesonide 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 Budesonide 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 Budesonide and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Budesonide NDC to their finished compounded human drug products, they may choose to do so.

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

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.