01 1CTX Lifesciences
02 1Lusochimica
03 1Siegfried AG
04 1Blank
01 1XYLOMETAZOLINE HCL
02 1XYLOMETAZOLINE HYDROCHLORIDE
03 1XYLOMETAZOLINE HYDROCHLORIDE USP
04 1XYLOMETAZOLINNE HYDROCHLORIDE
01 1India
02 1Italy
03 1Switzerland
04 1Blank
01 2Active
02 2Inactive
01 4Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 22045
Submission : 2008-09-19
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 2498
Submission : 1975-06-18
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 9104
Submission : 1991-05-15
Status : Active
Type : II
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 2691
Submission : 1976-05-27
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
59
PharmaCompass offers a list of Xylometazoline Hydrochloride 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 Xylometazoline Hydrochloride manufacturer or Xylometazoline Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Xylometazoline Hydrochloride manufacturer or Xylometazoline Hydrochloride supplier.
PharmaCompass also assists you with knowing the Xylometazoline Hydrochloride API Price utilized in the formulation of products. Xylometazoline Hydrochloride API Price is not always fixed or binding as the Xylometazoline Hydrochloride Price is obtained through a variety of data sources. The Xylometazoline Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Otriven manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Otriven, including repackagers and relabelers. The FDA regulates Otriven manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Otriven 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 Otriven manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Otriven supplier is an individual or a company that provides Otriven active pharmaceutical ingredient (API) or Otriven finished formulations upon request. The Otriven suppliers may include Otriven API manufacturers, exporters, distributors and traders.
click here to find a list of Otriven suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Otriven DMF (Drug Master File) is a document detailing the whole manufacturing process of Otriven active pharmaceutical ingredient (API) in detail. Different forms of Otriven DMFs exist exist since differing nations have different regulations, such as Otriven USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Otriven DMF submitted to regulatory agencies in the US is known as a USDMF. Otriven USDMF includes data on Otriven's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Otriven USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Otriven suppliers with USDMF on PharmaCompass.
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