Minakem delivers API, HPAPI, steroids & CDMO services for generics with FDA/GMP certification, regulatory know-how & proven success.
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
01 7BUDESONIDE
02 4BUDESONIDE MICRONIZED
03 18Budesonide
04 1Budesonide Micronised Co-Suspension APN
05 5Budesonide Micronized
06 1budesonide
01 2Canada
02 2China
03 2France
04 2Germany
05 5India
06 9Italy
07 1Malaysia
08 1Mexico
09 1Netherlands
10 8U.S.A
11 3United Kingdom
Minakem delivers API, HPAPI, steroids & CDMO services for generics with FDA/GMP certification, regulatory know-how & proven success.
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
Vamsi Labs is one of the major manufacturers of Anti-asthmatic, Anti-migraine & Anti-psychotic APIs.
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...
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
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
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
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
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
Minakem delivers API, HPAPI, steroids & CDMO services for generics with FDA/GMP certification, regulatory know-how & proven success.
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
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
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
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
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.
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.
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).
The FDA updates the NDC directory daily. The NDC numbers for Budesonide 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 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.
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.
We have 27 companies offering Budesonide
Get in contact with the supplier of your choice:
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