Chirogate is a professional Prostaglandin manufacturer.
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01 1Chirogate International
02 1EUROAPI
03 1BrightGene Bio-Medical Technology Co.,Ltd
04 1MSN Laboratories
05 1TIEN (Tianjin) Pharmaceutical
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01 4CARBOPROST TROMETHAMINE
02 1CARBOPROST TROMETHAMINE USP [ROUTE CODE "CE"]
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01 2China
02 1France
03 1India
04 1Taiwan
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01 5Active
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01 3Complete
02 2Blank
GDUFA
DMF Review : Complete
Rev. Date : 2020-12-01
Pay. Date : 2020-09-17
DMF Number : 33807
Submission : 2019-07-09
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2022-03-01
Pay. Date : 2022-02-11
DMF Number : 35412
Submission : 2021-11-15
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 37422
Submission : 2022-08-31
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2017-11-03
Pay. Date : 2017-10-06
DMF Number : 27865
Submission : 2014-01-27
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 36373
Submission : 2021-10-14
Status : Active
Type : II
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PharmaCompass offers a list of Carboprost Tromethamine 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 Carboprost Tromethamine manufacturer or Carboprost Tromethamine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Carboprost Tromethamine manufacturer or Carboprost Tromethamine supplier.
PharmaCompass also assists you with knowing the Carboprost Tromethamine API Price utilized in the formulation of products. Carboprost Tromethamine API Price is not always fixed or binding as the Carboprost Tromethamine Price is obtained through a variety of data sources. The Carboprost Tromethamine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 58551-69-2 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 58551-69-2, including repackagers and relabelers. The FDA regulates 58551-69-2 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 58551-69-2 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 58551-69-2 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A 58551-69-2 supplier is an individual or a company that provides 58551-69-2 active pharmaceutical ingredient (API) or 58551-69-2 finished formulations upon request. The 58551-69-2 suppliers may include 58551-69-2 API manufacturers, exporters, distributors and traders.
click here to find a list of 58551-69-2 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A 58551-69-2 DMF (Drug Master File) is a document detailing the whole manufacturing process of 58551-69-2 active pharmaceutical ingredient (API) in detail. Different forms of 58551-69-2 DMFs exist exist since differing nations have different regulations, such as 58551-69-2 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A 58551-69-2 DMF submitted to regulatory agencies in the US is known as a USDMF. 58551-69-2 USDMF includes data on 58551-69-2's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The 58551-69-2 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of 58551-69-2 suppliers with USDMF on PharmaCompass.
We have 5 companies offering 58551-69-2
Get in contact with the supplier of your choice: