01 1Acharya Chemicals
02 1India Phosphate
03 1Salvi Chemical Industries
01 2DRIED FERROUS SULFATE USP
02 1DRIED FERROUS SULPHATE USP
01 3India
01 3Active
01 3Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 31742
Submission : 2017-05-02
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 34465
Submission : 2020-01-31
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 29932
Submission : 2015-03-25
Status : Active
Type : II
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PharmaCompass offers a list of Ferrous Sulfate 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 Ferrous Sulfate manufacturer or Ferrous Sulfate supplier for your needs.
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PharmaCompass also assists you with knowing the Ferrous Sulfate API Price utilized in the formulation of products. Ferrous Sulfate API Price is not always fixed or binding as the Ferrous Sulfate Price is obtained through a variety of data sources. The Ferrous Sulfate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Tox21_202580 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tox21_202580, including repackagers and relabelers. The FDA regulates Tox21_202580 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tox21_202580 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_202580 supplier is an individual or a company that provides Tox21_202580 active pharmaceutical ingredient (API) or Tox21_202580 finished formulations upon request. The Tox21_202580 suppliers may include Tox21_202580 API manufacturers, exporters, distributors and traders.
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A Tox21_202580 DMF (Drug Master File) is a document detailing the whole manufacturing process of Tox21_202580 active pharmaceutical ingredient (API) in detail. Different forms of Tox21_202580 DMFs exist exist since differing nations have different regulations, such as Tox21_202580 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Tox21_202580 DMF submitted to regulatory agencies in the US is known as a USDMF. Tox21_202580 USDMF includes data on Tox21_202580's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Tox21_202580 USDMF is kept confidential to protect the manufacturer’s intellectual property.
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