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01 1Aurobindo Pharma Limited
02 1Navinta
03 1Sun Pharmaceutical Industries Limited
04 1Teva Pharmaceutical Industries
05 1Ultragenyx Pharmaceutical
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01 4TRIHEPTANOIN
02 1TRIHEPTANOIN ULTRAPURE
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01 2India
02 1Israel
03 2U.S.A
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01 5Active
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01 3Complete
02 2Blank
GDUFA
DMF Review : Complete
Rev. Date : 2024-03-21
Pay. Date : 2024-01-25
DMF Number : 39430
Submission : 2024-02-08
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2024-04-16
Pay. Date : 2024-03-22
DMF Number : 39441
Submission : 2024-03-26
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2024-04-16
Pay. Date : 2024-03-15
DMF Number : 39415
Submission : 2024-03-29
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 39145
Submission : 2024-02-07
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 26895
Submission : 2013-03-01
Status : Active
Type : II
95
PharmaCompass offers a list of Triheptanoin 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 Triheptanoin manufacturer or Triheptanoin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Triheptanoin manufacturer or Triheptanoin supplier.
PharmaCompass also assists you with knowing the Triheptanoin API Price utilized in the formulation of products. Triheptanoin API Price is not always fixed or binding as the Triheptanoin Price is obtained through a variety of data sources. The Triheptanoin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A TRIHEPTANOIN ULTRAPURE manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of TRIHEPTANOIN ULTRAPURE, including repackagers and relabelers. The FDA regulates TRIHEPTANOIN ULTRAPURE manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. TRIHEPTANOIN ULTRAPURE 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 TRIHEPTANOIN ULTRAPURE manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A TRIHEPTANOIN ULTRAPURE supplier is an individual or a company that provides TRIHEPTANOIN ULTRAPURE active pharmaceutical ingredient (API) or TRIHEPTANOIN ULTRAPURE finished formulations upon request. The TRIHEPTANOIN ULTRAPURE suppliers may include TRIHEPTANOIN ULTRAPURE API manufacturers, exporters, distributors and traders.
click here to find a list of TRIHEPTANOIN ULTRAPURE suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A TRIHEPTANOIN ULTRAPURE DMF (Drug Master File) is a document detailing the whole manufacturing process of TRIHEPTANOIN ULTRAPURE active pharmaceutical ingredient (API) in detail. Different forms of TRIHEPTANOIN ULTRAPURE DMFs exist exist since differing nations have different regulations, such as TRIHEPTANOIN ULTRAPURE USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A TRIHEPTANOIN ULTRAPURE DMF submitted to regulatory agencies in the US is known as a USDMF. TRIHEPTANOIN ULTRAPURE USDMF includes data on TRIHEPTANOIN ULTRAPURE's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The TRIHEPTANOIN ULTRAPURE USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of TRIHEPTANOIN ULTRAPURE suppliers with USDMF on PharmaCompass.
We have 5 companies offering TRIHEPTANOIN ULTRAPURE
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