01 1Curia
02 1Dishman Carbogen Amcis
03 2Blank
01 1ATROPINE/PRALIDOXIME CHLORIDE INJECTION (PERFORATED NEEDLE)
02 1ATROPINE/PRALIDOXIME CHLORIDE INJECTION (RETRACTION NEEDLE)
03 1PRALIDOXIME CHLORIDE
04 1PRALIDOXIME CHLORIDE USP
01 1India
02 1U.S.A
03 2Blank
01 2Active
02 2Inactive
01 4Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 14208
Submission : 1999-06-14
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 21307
Submission : 2008-02-04
Status : Active
Type : II
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 8750
Submission : 1990-09-17
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 8751
Submission : 1990-09-17
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
94
PharmaCompass offers a list of Pralidoxime Chloride 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 Pralidoxime Chloride manufacturer or Pralidoxime Chloride supplier for your needs.
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PharmaCompass also assists you with knowing the Pralidoxime Chloride API Price utilized in the formulation of products. Pralidoxime Chloride API Price is not always fixed or binding as the Pralidoxime Chloride Price is obtained through a variety of data sources. The Pralidoxime Chloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Pralidoxime Methyl Sulphate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Pralidoxime Methyl Sulphate, including repackagers and relabelers. The FDA regulates Pralidoxime Methyl Sulphate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Pralidoxime Methyl Sulphate 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 Pralidoxime Methyl Sulphate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Pralidoxime Methyl Sulphate supplier is an individual or a company that provides Pralidoxime Methyl Sulphate active pharmaceutical ingredient (API) or Pralidoxime Methyl Sulphate finished formulations upon request. The Pralidoxime Methyl Sulphate suppliers may include Pralidoxime Methyl Sulphate API manufacturers, exporters, distributors and traders.
click here to find a list of Pralidoxime Methyl Sulphate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Pralidoxime Methyl Sulphate DMF (Drug Master File) is a document detailing the whole manufacturing process of Pralidoxime Methyl Sulphate active pharmaceutical ingredient (API) in detail. Different forms of Pralidoxime Methyl Sulphate DMFs exist exist since differing nations have different regulations, such as Pralidoxime Methyl Sulphate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Pralidoxime Methyl Sulphate DMF submitted to regulatory agencies in the US is known as a USDMF. Pralidoxime Methyl Sulphate USDMF includes data on Pralidoxime Methyl Sulphate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Pralidoxime Methyl Sulphate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Pralidoxime Methyl Sulphate suppliers with USDMF on PharmaCompass.
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