01 1F. Hoffmann-La Roche
02 1India Phosphate
03 1Mallinckrodt Pharmaceuticals
04 1Polydrug Laboratories Private Limited
05 1Salvi Chemical Industries
06 1Shree Vardhan Industries
01 1DESTAB(TM) FERROUS FUMARATE 90 S ULTRA
02 1FERROUS FUMARATE
03 1FERROUS FUMARATE "TOLERON"
04 3FERROUS FUMARATE USP
01 4India
02 1Ireland
03 1Switzerland
01 3Active
02 3Inactive
01 6Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 17321
Submission : 2004-04-16
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 33135
Submission : 2018-11-23
Status : Active
Type : IV
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 211
Submission : 1940-01-01
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 24184
Submission : 2010-09-13
Status : Inactive
Type : IV
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 29276
Submission : 2015-03-25
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 34498
Submission : 2021-02-12
Status : Active
Type : II
22
PharmaCompass offers a list of Ferrous Fumarate 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 Fumarate manufacturer or Ferrous Fumarate supplier for your needs.
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PharmaCompass also assists you with knowing the Ferrous Fumarate API Price utilized in the formulation of products. Ferrous Fumarate API Price is not always fixed or binding as the Ferrous Fumarate Price is obtained through a variety of data sources. The Ferrous Fumarate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A LO-BLISOVI FE-2 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of LO-BLISOVI FE-2, including repackagers and relabelers. The FDA regulates LO-BLISOVI FE-2 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. LO-BLISOVI FE-2 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 LO-BLISOVI FE-2 supplier is an individual or a company that provides LO-BLISOVI FE-2 active pharmaceutical ingredient (API) or LO-BLISOVI FE-2 finished formulations upon request. The LO-BLISOVI FE-2 suppliers may include LO-BLISOVI FE-2 API manufacturers, exporters, distributors and traders.
click here to find a list of LO-BLISOVI FE-2 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A LO-BLISOVI FE-2 DMF (Drug Master File) is a document detailing the whole manufacturing process of LO-BLISOVI FE-2 active pharmaceutical ingredient (API) in detail. Different forms of LO-BLISOVI FE-2 DMFs exist exist since differing nations have different regulations, such as LO-BLISOVI FE-2 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A LO-BLISOVI FE-2 DMF submitted to regulatory agencies in the US is known as a USDMF. LO-BLISOVI FE-2 USDMF includes data on LO-BLISOVI FE-2's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The LO-BLISOVI FE-2 USDMF is kept confidential to protect the manufacturer’s intellectual property.
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We have 6 companies offering LO-BLISOVI FE-2
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