China's leading API and intermediate manufacturer, offering CMO/CDMO services and exports to 70+ countries, enhancing global health.
01 1Shandong Chenghui Shuangda Pharmaceutical
02 1Changzhou Tianhua Pharmaceutical Co.,Ltd
03 1Venkata Narayana Active Ingredients
01 2TETRACAINE
02 1TETRACAINE USP
01 2China
02 1India
01 3Active
01 1Complete
02 2Blank
China's leading API and intermediate manufacturer, offering CMO/CDMO services and exports to 70+ countries, enhancing global health.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 35615
Submission : 2021-02-04
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 22496
Submission : 2008-12-31
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2018-10-30
Pay. Date : 2018-09-12
DMF Number : 24100
Submission : 2010-08-26
Status : Active
Type : II
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PharmaCompass offers a list of Tetracaine 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 Tetracaine manufacturer or Tetracaine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Tetracaine manufacturer or Tetracaine supplier.
PharmaCompass also assists you with knowing the Tetracaine API Price utilized in the formulation of products. Tetracaine API Price is not always fixed or binding as the Tetracaine Price is obtained through a variety of data sources. The Tetracaine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 0619F35CGV manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 0619F35CGV, including repackagers and relabelers. The FDA regulates 0619F35CGV manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 0619F35CGV API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A 0619F35CGV supplier is an individual or a company that provides 0619F35CGV active pharmaceutical ingredient (API) or 0619F35CGV finished formulations upon request. The 0619F35CGV suppliers may include 0619F35CGV API manufacturers, exporters, distributors and traders.
click here to find a list of 0619F35CGV suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A 0619F35CGV DMF (Drug Master File) is a document detailing the whole manufacturing process of 0619F35CGV active pharmaceutical ingredient (API) in detail. Different forms of 0619F35CGV DMFs exist exist since differing nations have different regulations, such as 0619F35CGV USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A 0619F35CGV DMF submitted to regulatory agencies in the US is known as a USDMF. 0619F35CGV USDMF includes data on 0619F35CGV's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The 0619F35CGV USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of 0619F35CGV suppliers with USDMF on PharmaCompass.
We have 3 companies offering 0619F35CGV
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