01 1Chongqing Carelife Pharmaceutical
02 1Hetero Drugs
03 2MSN Laboratories
04 1Zhejiang Huayi Pharmaceutical Co., Ltd.
01 3REGORAFENIB
02 1REGORAFENIB MONOHYDRATE USP
03 1REGORAFENIB [ROUTE CODE "RZ"]
01 2China
02 3India
01 5Active
01 3Complete
02 2Blank
GDUFA
DMF Review : Complete
Rev. Date : 2023-08-14
Pay. Date : 2023-05-08
DMF Number : 38197
Submission : 2023-04-26
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2016-07-06
Pay. Date : 2016-05-02
DMF Number : 30490
Submission : 2016-05-13
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 36838
Submission : 2022-03-30
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2016-01-21
Pay. Date : 2015-11-06
DMF Number : 29870
Submission : 2015-11-03
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 39898
Submission : 2024-04-27
Status : Active
Type : II
82
PharmaCompass offers a list of Regorafenib 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 Regorafenib manufacturer or Regorafenib supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Regorafenib manufacturer or Regorafenib supplier.
PharmaCompass also assists you with knowing the Regorafenib API Price utilized in the formulation of products. Regorafenib API Price is not always fixed or binding as the Regorafenib Price is obtained through a variety of data sources. The Regorafenib Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Stivarga manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Stivarga, including repackagers and relabelers. The FDA regulates Stivarga manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Stivarga 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 Stivarga manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Stivarga supplier is an individual or a company that provides Stivarga active pharmaceutical ingredient (API) or Stivarga finished formulations upon request. The Stivarga suppliers may include Stivarga API manufacturers, exporters, distributors and traders.
click here to find a list of Stivarga suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Stivarga DMF (Drug Master File) is a document detailing the whole manufacturing process of Stivarga active pharmaceutical ingredient (API) in detail. Different forms of Stivarga DMFs exist exist since differing nations have different regulations, such as Stivarga USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Stivarga DMF submitted to regulatory agencies in the US is known as a USDMF. Stivarga USDMF includes data on Stivarga's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Stivarga USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Stivarga suppliers with USDMF on PharmaCompass.
We have 4 companies offering Stivarga
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