EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
01 1Aventis Pharma Manufacturing Pte Ltd.
02 1EUROAPI FRANCE
03 1Fermion Oy
04 1AX Pharmaceutical Corp
05 1Cambrex Profarmaco Milano Srl
06 1Changzhou Tianhua Pharmaceutical Co. Ltd.
07 1DARMERICA, LLC
08 1Fagron Inc
09 1Fagron Services B.V.
10 1LETCO MEDICAL, LLC
11 1Medisca Inc.
12 1Olon SpA
13 1Professional Compounding Centers of America
14 1Spectrum Laboratory Products, Inc.
15 1Yumen Qianhua Pharmaceutical Co., Ltd.
01 4CROMOLYN SODIUM
02 10Cromolyn Sodium
03 1Cromolyn sodium
01 1Canada
02 1China
03 1Finland
04 2France
05 1Italy
06 2Netherlands
07 5U.S.A
08 1United Kingdom
09 1Blank
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
NDC Package Code : 62255-1321
Start Marketing Date : 2017-01-13
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
With Fermion, start the journey of your innovative API.
NDC Package Code : 12780-4960
Start Marketing Date : 1997-01-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
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
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
NDC Package Code : 51552-0423
Start Marketing Date : 1998-04-01
End Marketing Date : 2027-07-13
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 62991-1038
Start Marketing Date : 2011-04-22
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 38779-0301
Start Marketing Date : 2014-08-04
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17337-0511
Start Marketing Date : 2017-02-10
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-5178
Start Marketing Date : 2022-04-11
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 49452-0006
Start Marketing Date : 2000-07-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
A Cromolyn Sodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cromolyn Sodium, including repackagers and relabelers. The FDA regulates Cromolyn Sodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cromolyn Sodium 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 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cromolyn Sodium supplier is an individual or a company that provides Cromolyn Sodium active pharmaceutical ingredient (API) or Cromolyn Sodium finished formulations upon request. The Cromolyn Sodium suppliers may include Cromolyn Sodium API manufacturers, exporters, distributors and traders.
click here to find a list of Cromolyn Sodium 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 Cromolyn Sodium as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Cromolyn Sodium 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 Cromolyn Sodium 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 Cromolyn Sodium and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Cromolyn Sodium NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Cromolyn Sodium suppliers with NDC on PharmaCompass.
We have 12 companies offering Cromolyn Sodium
Get in contact with the supplier of your choice:
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