01 3GSK
01 2TICARCILLIN DISODIUM
02 1TICARCILLIN DISODIUM BULK (STERILE )
01 3United Kingdom
01 3Inactive
01 3Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13570
Submission : 1998-09-01
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 16076
Submission : 2002-07-31
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 14959
Submission : 2000-07-28
Status : Inactive
Type : II
73
PharmaCompass offers a list of Ticarcillin 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 Ticarcillin manufacturer or Ticarcillin supplier for your needs.
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PharmaCompass also assists you with knowing the Ticarcillin API Price utilized in the formulation of products. Ticarcillin API Price is not always fixed or binding as the Ticarcillin Price is obtained through a variety of data sources. The Ticarcillin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A TIMENTIN-1 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of TIMENTIN-1, including repackagers and relabelers. The FDA regulates TIMENTIN-1 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. TIMENTIN-1 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 TIMENTIN-1 supplier is an individual or a company that provides TIMENTIN-1 active pharmaceutical ingredient (API) or TIMENTIN-1 finished formulations upon request. The TIMENTIN-1 suppliers may include TIMENTIN-1 API manufacturers, exporters, distributors and traders.
click here to find a list of TIMENTIN-1 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A TIMENTIN-1 DMF (Drug Master File) is a document detailing the whole manufacturing process of TIMENTIN-1 active pharmaceutical ingredient (API) in detail. Different forms of TIMENTIN-1 DMFs exist exist since differing nations have different regulations, such as TIMENTIN-1 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A TIMENTIN-1 DMF submitted to regulatory agencies in the US is known as a USDMF. TIMENTIN-1 USDMF includes data on TIMENTIN-1's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The TIMENTIN-1 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of TIMENTIN-1 suppliers with USDMF on PharmaCompass.
