01 2MSN Laboratories
02 1Shilpa Medicare
03 1Synthon Pharmaceuticals
04 1Wisdom Pharmaceutical
05 1Zhejiang Jiuzhou Pharmaceutical
01 4AXITINIB
02 1AXITINIB (FORM-XLI)[ROUTE CODE - "XB"]
03 1AXITINIB [ROUTE CODE - "XA"]
01 2China
02 3India
03 1Netherlands
01 6Active
01 5Complete
02 1Blank
GDUFA
DMF Review : Complete
Rev. Date : 2016-09-16
Pay. Date : 2016-07-01
DMF Number : 30341
Submission : 2016-03-04
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2015-12-18
Pay. Date : 2015-09-23
DMF Number : 29672
Submission : 2015-09-29
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2016-02-05
Pay. Date : 2015-12-23
DMF Number : 30104
Submission : 2015-12-24
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2023-06-27
Pay. Date : 2023-02-06
DMF Number : 37971
Submission : 2023-02-02
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 39323
Submission : 2023-12-27
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2016-04-15
Pay. Date : 2015-10-29
DMF Number : 29918
Submission : 2015-10-10
Status : Active
Type : II
53
PharmaCompass offers a list of Axitinib 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 Axitinib manufacturer or Axitinib supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Axitinib manufacturer or Axitinib supplier.
PharmaCompass also assists you with knowing the Axitinib API Price utilized in the formulation of products. Axitinib API Price is not always fixed or binding as the Axitinib Price is obtained through a variety of data sources. The Axitinib Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A AG-13736 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of AG-13736, including repackagers and relabelers. The FDA regulates AG-13736 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. AG-13736 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 AG-13736 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A AG-13736 supplier is an individual or a company that provides AG-13736 active pharmaceutical ingredient (API) or AG-13736 finished formulations upon request. The AG-13736 suppliers may include AG-13736 API manufacturers, exporters, distributors and traders.
click here to find a list of AG-13736 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A AG-13736 DMF (Drug Master File) is a document detailing the whole manufacturing process of AG-13736 active pharmaceutical ingredient (API) in detail. Different forms of AG-13736 DMFs exist exist since differing nations have different regulations, such as AG-13736 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A AG-13736 DMF submitted to regulatory agencies in the US is known as a USDMF. AG-13736 USDMF includes data on AG-13736's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The AG-13736 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of AG-13736 suppliers with USDMF on PharmaCompass.
We have 5 companies offering AG-13736
Get in contact with the supplier of your choice:
