With Fermion, start the journey of your innovative API.
01 1Fermion Oy
02 1Lusochimica
03 2Plantex Ltd.
04 1Souvin Pharmaceuticals Pvt. Ltd
01 1TOLNAFTATE
02 1TOLNAFTATE U.S.P.
03 2TOLNAFTATE USP
04 1TOLNAFTATE USP XX
01 1Finland
02 1India
03 2Israel
04 1Italy
01 1Active
02 4Inactive
01 5Blank
With Fermion, start the journey of your innovative API.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 5796
Submission : 1985-04-03
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 5427
Submission : 1984-07-09
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3087
Submission : 1977-11-22
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3041
Submission : 1977-10-24
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 26761
Submission : 2012-12-20
Status : Inactive
Type : II
24
PharmaCompass offers a list of Tolnaftate 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 Tolnaftate manufacturer or Tolnaftate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Tolnaftate manufacturer or Tolnaftate supplier.
PharmaCompass also assists you with knowing the Tolnaftate API Price utilized in the formulation of products. Tolnaftate API Price is not always fixed or binding as the Tolnaftate Price is obtained through a variety of data sources. The Tolnaftate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Zeasorb-AF powder manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Zeasorb-AF powder, including repackagers and relabelers. The FDA regulates Zeasorb-AF powder manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Zeasorb-AF powder 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 Zeasorb-AF powder manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Zeasorb-AF powder supplier is an individual or a company that provides Zeasorb-AF powder active pharmaceutical ingredient (API) or Zeasorb-AF powder finished formulations upon request. The Zeasorb-AF powder suppliers may include Zeasorb-AF powder API manufacturers, exporters, distributors and traders.
click here to find a list of Zeasorb-AF powder suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Zeasorb-AF powder DMF (Drug Master File) is a document detailing the whole manufacturing process of Zeasorb-AF powder active pharmaceutical ingredient (API) in detail. Different forms of Zeasorb-AF powder DMFs exist exist since differing nations have different regulations, such as Zeasorb-AF powder USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Zeasorb-AF powder DMF submitted to regulatory agencies in the US is known as a USDMF. Zeasorb-AF powder USDMF includes data on Zeasorb-AF powder's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Zeasorb-AF powder USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Zeasorb-AF powder suppliers with USDMF on PharmaCompass.
We have 4 companies offering Zeasorb-AF powder
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