01 1Recordati
02 1Shanghai Wonder Pharmaceutical
03 2Blank
01 3DIMENHYDRINATE
02 1DIMENHYDRINATE, BULK POWDER FORM
01 1China
02 1Italy
03 2Blank
01 2Active
02 2Inactive
01 4Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 4627
Submission : 1982-07-13
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 31353
Submission : 2017-02-06
Status : Active
Type : II
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 2898
Submission : 1977-04-14
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 : 4615
Submission : 1982-07-22
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
63
PharmaCompass offers a list of Dimenhydrinate 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 Dimenhydrinate manufacturer or Dimenhydrinate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Dimenhydrinate manufacturer or Dimenhydrinate supplier.
PharmaCompass also assists you with knowing the Dimenhydrinate API Price utilized in the formulation of products. Dimenhydrinate API Price is not always fixed or binding as the Dimenhydrinate Price is obtained through a variety of data sources. The Dimenhydrinate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Xamamina manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Xamamina, including repackagers and relabelers. The FDA regulates Xamamina manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Xamamina 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 Xamamina manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Xamamina supplier is an individual or a company that provides Xamamina active pharmaceutical ingredient (API) or Xamamina finished formulations upon request. The Xamamina suppliers may include Xamamina API manufacturers, exporters, distributors and traders.
click here to find a list of Xamamina suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Xamamina DMF (Drug Master File) is a document detailing the whole manufacturing process of Xamamina active pharmaceutical ingredient (API) in detail. Different forms of Xamamina DMFs exist exist since differing nations have different regulations, such as Xamamina USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Xamamina DMF submitted to regulatory agencies in the US is known as a USDMF. Xamamina USDMF includes data on Xamamina's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Xamamina USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Xamamina suppliers with USDMF on PharmaCompass.
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