Curia - Accelerating therapies from discovery to commercialization with flexible, scalable CDMO solutions.
01 1Curia
02 1Dr. Reddy's Laboratories
03 1Moehs Iberica
04 1Alivus Life Sciences
05 1Changzhou Pharmaceutical Factory
06 1Chiral Quest
07 1Cipla
08 1Zydus Lifesciences
09 1Blank
Curia - Accelerating therapies from discovery to commercialization with flexible, scalable CDMO solutions.
GDUFA
DMF Review : Complete
Rev. Date : 2025-04-23
Pay. Date : 2025-04-04
DMF Number : 41626
Submission : 2025-03-28
Status :
Type : II
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 41452
Submission : 2025-03-28
Status :
Type : II
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 41294
Submission : 2025-02-12
Status :
Type : II
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PharmaCompass offers a list of Deucravacitinib 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 Deucravacitinib manufacturer or Deucravacitinib supplier for your needs.
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A Deucravacitinib manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Deucravacitinib, including repackagers and relabelers. The FDA regulates Deucravacitinib manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Deucravacitinib 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 Deucravacitinib manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Deucravacitinib supplier is an individual or a company that provides Deucravacitinib active pharmaceutical ingredient (API) or Deucravacitinib finished formulations upon request. The Deucravacitinib suppliers may include Deucravacitinib API manufacturers, exporters, distributors and traders.
click here to find a list of Deucravacitinib suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Deucravacitinib DMF (Drug Master File) is a document detailing the whole manufacturing process of Deucravacitinib active pharmaceutical ingredient (API) in detail. Different forms of Deucravacitinib DMFs exist exist since differing nations have different regulations, such as Deucravacitinib USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Deucravacitinib DMF submitted to regulatory agencies in the US is known as a USDMF. Deucravacitinib USDMF includes data on Deucravacitinib's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Deucravacitinib USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Deucravacitinib suppliers with USDMF on PharmaCompass.
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