01 1Medimpex
02 1RP SCHERER GMBH & CO. KG
03 3Blank
01 1DIHYDROERGOTOXIN METHANESULPHONATE
02 1DIHYDROERGOTOXINE MESYLATE
03 1DIHYDROERGOTOXINE METHANE SULFONATE
04 1DIHYDROERGOTOXINE METHANESULFONATE (ERGOLOID MESYLATES)
05 1HYDERGINE(ERGOLOID MESYLATES) 1MG SOFTGELS
01 1Germany
02 1United Kingdom
03 3Blank
01 5Inactive
01 5Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 2548
Submission : 1975-10-31
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 15415
Submission : 2001-05-04
Status : Inactive
Type : II
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 2699
Submission : 1976-06-10
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 : 3022
Submission : 1977-09-23
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 : 2947
Submission : 1977-05-13
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
28
PharmaCompass offers a list of Dihydroergotoxine Mesylate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Dihydroergotoxine Mesylate manufacturer or Dihydroergotoxine Mesylate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Dihydroergotoxine Mesylate manufacturer or Dihydroergotoxine Mesylate supplier.
A Redergin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Redergin, including repackagers and relabelers. The FDA regulates Redergin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Redergin 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 Redergin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Redergin supplier is an individual or a company that provides Redergin active pharmaceutical ingredient (API) or Redergin finished formulations upon request. The Redergin suppliers may include Redergin API manufacturers, exporters, distributors and traders.
click here to find a list of Redergin suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Redergin DMF (Drug Master File) is a document detailing the whole manufacturing process of Redergin active pharmaceutical ingredient (API) in detail. Different forms of Redergin DMFs exist exist since differing nations have different regulations, such as Redergin USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Redergin DMF submitted to regulatory agencies in the US is known as a USDMF. Redergin USDMF includes data on Redergin's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Redergin USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Redergin suppliers with USDMF on PharmaCompass.
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