01 1Anmol Chemicals
02 1GE Healthcare Inc
03 1Jungbunzlauer International AG
04 1Muby Chemicals
05 1Blank
01 2ANHYDROUS CITRIC ACID
02 1CITRIC ACID ANHYDROUS USP
03 1CITRIC ACID MONOHYDRATE USP
04 1FASTLAB FDG CITRATE CASSETTE PACK
01 2India
02 1Switzerland
03 1United Kingdom
04 1Blank
01 5Active
01 1Complete
02 4Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 40739
Submission : 2025-01-09
Status : Active
Type : IV
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 25371
Submission : 2011-10-07
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2013-10-07
Pay. Date : 2013-09-27
DMF Number : 23078
Submission : 2009-08-28
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 40763
Submission : 2024-11-04
Status : Active
Type : II
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 41162
Submission : 2025-01-03
Status : Active
Type : IV
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
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PharmaCompass offers a list of Citric Acid 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 Citric Acid manufacturer or Citric Acid supplier for your needs.
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A Tox21_202405 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tox21_202405, including repackagers and relabelers. The FDA regulates Tox21_202405 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tox21_202405 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Tox21_202405 supplier is an individual or a company that provides Tox21_202405 active pharmaceutical ingredient (API) or Tox21_202405 finished formulations upon request. The Tox21_202405 suppliers may include Tox21_202405 API manufacturers, exporters, distributors and traders.
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A Tox21_202405 DMF (Drug Master File) is a document detailing the whole manufacturing process of Tox21_202405 active pharmaceutical ingredient (API) in detail. Different forms of Tox21_202405 DMFs exist exist since differing nations have different regulations, such as Tox21_202405 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Tox21_202405 DMF submitted to regulatory agencies in the US is known as a USDMF. Tox21_202405 USDMF includes data on Tox21_202405's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Tox21_202405 USDMF is kept confidential to protect the manufacturer’s intellectual property.
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We have 4 companies offering Tox21_202405
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