01 1Cadila Pharmaceuticals
02 1Cyalume Specialty Products
03 1Mallinckrodt Pharmaceuticals
04 1Siegfried AG
01 1D-PSEUDOEPHEDRINE FOR TIME RELEASE BEAD
02 1PSEUDOEPHEDRINE
03 2PSEUDOEPHEDRINE TANNATE
01 1India
02 1Ireland
03 1Switzerland
04 1U.S.A
01 2Active
02 2Inactive
01 1Complete
02 3Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 20819
Submission : 2007-08-06
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 23482
Submission : 2010-01-26
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3620
Submission : 1979-09-06
Status : Inactive
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2013-02-05
Pay. Date : 2013-01-24
DMF Number : 4185
Submission : 1981-05-27
Status : Active
Type : II
91
PharmaCompass offers a list of Pseudoephedrine 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 Pseudoephedrine manufacturer or Pseudoephedrine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Pseudoephedrine manufacturer or Pseudoephedrine supplier.
PharmaCompass also assists you with knowing the Pseudoephedrine API Price utilized in the formulation of products. Pseudoephedrine API Price is not always fixed or binding as the Pseudoephedrine Price is obtained through a variety of data sources. The Pseudoephedrine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Pseudo manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Pseudo, including repackagers and relabelers. The FDA regulates Pseudo manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Pseudo 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 Pseudo manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Pseudo supplier is an individual or a company that provides Pseudo active pharmaceutical ingredient (API) or Pseudo finished formulations upon request. The Pseudo suppliers may include Pseudo API manufacturers, exporters, distributors and traders.
click here to find a list of Pseudo suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Pseudo DMF (Drug Master File) is a document detailing the whole manufacturing process of Pseudo active pharmaceutical ingredient (API) in detail. Different forms of Pseudo DMFs exist exist since differing nations have different regulations, such as Pseudo USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Pseudo DMF submitted to regulatory agencies in the US is known as a USDMF. Pseudo USDMF includes data on Pseudo's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Pseudo USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Pseudo suppliers with USDMF on PharmaCompass.
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