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GDUFA
DMF Review : Reviewed
Rev. Date : 2018-06-13
Pay. Date : 2018-02-08
DMF Number : 10006
Submission : 1992-12-15
Status : Active
Type : II
Certificate Number : CEP 2013-136 - Rev 01
Issue Date : 2025-03-20
Type : Chemical
Substance Number : 562
Status : Valid
Registration Number : 223MF10083
Registrant's Address : Koivu-Mankkaan tie 6A, FI-02200 Espoo, Finland
Initial Date of Registration : 2011-06-17
Latest Date of Registration :
NDC Package Code : 12780-4960
Start Marketing Date : 1997-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Available Reg Filing : CN |
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-03-07
Pay. Date : 2013-02-25
DMF Number : 15890
Submission : 2002-03-08
Status : Active
Type : II
Certificate Number : R1-CEP 2001-421 - Rev 03
Issue Date : 2019-05-03
Type : Chemical
Substance Number : 562
Status : Valid
NDC Package Code : 82298-910
Start Marketing Date : 2017-01-13
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Certificate Number : R0-CEP 1999-199 - Rev 01
Issue Date : 2004-10-06
Type : Chemical
Substance Number : 562
Status : Withdrawn by Holder
Metrochem has been delivering customized volume & quality products to customers across the world, taking utmost care of their needs.
GDUFA
DMF Review : Reviewed
Rev. Date : 2019-04-03
Pay. Date : 2019-03-28
DMF Number : 8234
Submission : 1989-10-01
Status : Active
Type : II
Registration Number : 219MF10274
Registrant's Address : Strada Rivoltana Km 6/7 20053 Rodano Milano Italy
Initial Date of Registration : 2007-09-04
Latest Date of Registration :
GDUFA
DMF Review : Reviewed
Rev. Date : 2023-01-12
Pay. Date : 2023-01-06
DMF Number : 37598
Submission : 2022-12-28
Status : Active
Type : II
Certificate Number : CEP 2023-048 - Rev 00
Issue Date : 2024-08-12
Type : Chemical
Substance Number : 562
Status : Valid
NDC Package Code : 42571-445
Start Marketing Date : 2025-06-12
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (10kg/10kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 8164
Submission : 1989-08-02
Status : Active
Type : II
Certificate Number : CEP 2006-055 - Rev 03
Issue Date : 2024-02-19
Type : Chemical
Substance Number : 562
Status : Valid
Registration Number : 217MF11184
Registrant's Address : Via Curiel 34, 20067 Paulo, Milano, ITALY
Initial Date of Registration : 2005-12-12
Latest Date of Registration :
NDC Package Code : 12828-0062
Start Marketing Date : 1993-02-17
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 10736
Submission : 1994-02-18
Status : Inactive
Type : II
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 6815
Submission : 1987-02-04
Status : Inactive
Type : II
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PharmaCompass offers a list of Sodium Cromoglicate 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 Sodium Cromoglicate manufacturer or Sodium Cromoglicate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sodium Cromoglicate manufacturer or Sodium Cromoglicate supplier.
PharmaCompass also assists you with knowing the Sodium Cromoglicate API Price utilized in the formulation of products. Sodium Cromoglicate API Price is not always fixed or binding as the Sodium Cromoglicate Price is obtained through a variety of data sources. The Sodium Cromoglicate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cromolyn sodium (USP) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cromolyn sodium (USP), including repackagers and relabelers. The FDA regulates Cromolyn sodium (USP) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cromolyn sodium (USP) 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 Cromolyn sodium (USP) manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cromolyn sodium (USP) supplier is an individual or a company that provides Cromolyn sodium (USP) active pharmaceutical ingredient (API) or Cromolyn sodium (USP) finished formulations upon request. The Cromolyn sodium (USP) suppliers may include Cromolyn sodium (USP) API manufacturers, exporters, distributors and traders.
click here to find a list of Cromolyn sodium (USP) suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
We have 18 companies offering Cromolyn sodium (USP)
Get in contact with the supplier of your choice: