PMC Isochem is your partner for smart CDMOs of Intermediates, APIs, & excipients & a catalog of Intermediates & Generic APIs.
01 1PMC Isochem
02 1TAPI Technology & API Services
03 1Aurobindo Pharma Limited
04 1Cadila Pharmaceuticals
05 1Hikal
06 1Piramal Pharma Solutions
07 1Recordati
08 1SIMS Srl
09 1Shandong Weifang Pharma Factory Co., Ltd
10 1Shanghai Ziyuan Pharmaceutical
11 1Siegfried AG
12 2Signa S.A. de C.V.
13 1Zhejiang Excel Pharmaceutical
14 5Blank
PMC Isochem is your partner for smart CDMOs of Intermediates, APIs, & excipients & a catalog of Intermediates & Generic APIs.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 18056
Submission : 2005-02-03
Status :
Type : II
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 7445
Submission : 1988-04-22
Status :
Type : II
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PharmaCompass offers a list of Gemfibrozil 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 Gemfibrozil manufacturer or Gemfibrozil supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Gemfibrozil manufacturer or Gemfibrozil supplier.
PharmaCompass also assists you with knowing the Gemfibrozil API Price utilized in the formulation of products. Gemfibrozil API Price is not always fixed or binding as the Gemfibrozil Price is obtained through a variety of data sources. The Gemfibrozil Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A KBio3_001280 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of KBio3_001280, including repackagers and relabelers. The FDA regulates KBio3_001280 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. KBio3_001280 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 KBio3_001280 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A KBio3_001280 supplier is an individual or a company that provides KBio3_001280 active pharmaceutical ingredient (API) or KBio3_001280 finished formulations upon request. The KBio3_001280 suppliers may include KBio3_001280 API manufacturers, exporters, distributors and traders.
click here to find a list of KBio3_001280 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A KBio3_001280 DMF (Drug Master File) is a document detailing the whole manufacturing process of KBio3_001280 active pharmaceutical ingredient (API) in detail. Different forms of KBio3_001280 DMFs exist exist since differing nations have different regulations, such as KBio3_001280 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A KBio3_001280 DMF submitted to regulatory agencies in the US is known as a USDMF. KBio3_001280 USDMF includes data on KBio3_001280's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The KBio3_001280 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of KBio3_001280 suppliers with USDMF on PharmaCompass.
We have 13 companies offering KBio3_001280
Get in contact with the supplier of your choice:
