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

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01 4Minakem
02 1Vamsi Labs
03 2Coral Drugs Private Limited
04 3Axplora
05 1Minakem (formerly Delmar Chemicals)
06 1Transo-Pharm USA LLC
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08 1Aspen API
09 4Fermion Oy
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Minakem delivers API, HPAPI, steroids & CDMO services for generics with FDA/GMP certification, regulatory know-how & proven success.
GDUFA
DMF Review : Reviewed
Rev. Date : 2017-03-03
Pay. Date : 2017-02-10
DMF Number : 28441
Submission : 2014-06-20
Status : Active
Type : II
Registration Number : 301MF10045
Registrant's Address : 224 avenue de la Dordogne Zone d'Entreprises du Nord Gracht 59640 Dunkerque, France
Initial Date of Registration : 2019-08-20
Latest Date of Registration :
NDC Package Code : 49927-0004
Start Marketing Date : 2006-02-16
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Daewoong Pharmaceutical Co., Ltd.
Registration Date : 2023-07-19
Registration Number : 20221124-209-J-1409(A)
Manufacturer Name : Minakem Dunkerque production
Manufacturer Address : 224 avenue de la Dordogne Zone d'entreprises du Nord Gracht Dunkerque, 59640, France
| Available Reg Filing : ID, CN |
Vamsi Labs is one of the major manufacturers of Anti-asthmatic, Anti-migraine & Anti-psychotic APIs.
Certificate Number : CEP 2024-441 - Rev 00
Issue Date : 2025-12-10
Type : Chemical
Substance Number : 1075
Status : Valid
Date of Issue : 2025-11-12
Valid Till : 2028-07-02
Written Confirmation Number : WC-0155
Address of the Firm :
NDC Package Code : 66412-0393
Start Marketing Date : 2021-01-05
End Marketing Date : 2027-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
Registrant Name : Sanil Pharma Co., Ltd.
Registration Date : 2025-05-16
Registration Number : 20250516-209-J-1865
Manufacturer Name : Vamsi Labs Ltd.
Manufacturer Address : A-14, A-15, A-31, A-32 & A-33, MIDC Area, Chincholi, Tal- Mohol, Dist Solapur 413255, Maharashtra State, India
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 30534
Submission : 2017-02-02
Status : Active
Type : II
Certificate Number : CEP 2016-020 - Rev 01
Issue Date : 2026-01-06
Type : Chemical
Substance Number : 1075
Status : Valid
Date of Issue : 2025-11-20
Valid Till : 2028-11-19
Written Confirmation Number : WC-0009
Address of the Firm :
NDC Package Code : 49076-6111
Start Marketing Date : 2017-11-02
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-05-16
Pay. Date : 2013-05-03
DMF Number : 18910
Submission : 2005-10-26
Status : Active
Type : II
Certificate Number : R1-CEP 2000-051 - Rev 02
Issue Date : 2010-05-04
Type : Chemical
Substance Number : 1075
Status : Valid
NDC Package Code : 46439-8780
Start Marketing Date : 2025-02-14
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
Registrant Name : Sam-O Pharmaceutical Co., Ltd.
Registration Date : 2020-06-01
Registration Number : 20200601-209-J-448
Manufacturer Name : Farmabios SpA@Microchem Srl
Manufacturer Address : 27027, via Pavia 1, GROPELLO CAIROLI-(PV), Italy@Via Turati, 2-29017 Fiorenzuola D'arda (PC), Italy
| Available Reg Filing : SAU |
LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
NDC Package Code : 60870-0466
Start Marketing Date : 1993-09-23
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
Certificate Number : CEP 2023-318 - Rev 00
Issue Date : 2024-09-25
Type : Chemical
Substance Number : 1075
Status : Valid
Metrochem has been delivering customized volume & quality products to customers across the world, taking utmost care of their needs.
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PharmaCompass offers a list of Budesonide API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Budesonide manufacturer or Budesonide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Budesonide manufacturer or Budesonide supplier.
A Pulmicort Flexhaler manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Pulmicort Flexhaler, including repackagers and relabelers. The FDA regulates Pulmicort Flexhaler manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Pulmicort Flexhaler 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 Pulmicort Flexhaler manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Pulmicort Flexhaler supplier is an individual or a company that provides Pulmicort Flexhaler active pharmaceutical ingredient (API) or Pulmicort Flexhaler finished formulations upon request. The Pulmicort Flexhaler suppliers may include Pulmicort Flexhaler API manufacturers, exporters, distributors and traders.
click here to find a list of Pulmicort Flexhaler suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
We have 65 companies offering Pulmicort Flexhaler
Get in contact with the supplier of your choice: