Bloomage is a one-stop source for CEP Sodium Hyaluronate and Hyaluronic Acid// FDA-inspected & GMP-certified.

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01 1Bloomage Biotechnology Corp., Ltd
02 1Shandong Freda Biotechnology
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01 1ECTOINE
02 1ECTOINE (ECTOINE-200)
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01 2China
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01 2Active
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01 2Blank
Bloomage is a one-stop source for CEP Sodium Hyaluronate and Hyaluronic Acid// FDA-inspected & GMP-certified.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 37812
Submission : 2022-12-30
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 38868
Submission : 2023-09-18
Status : Active
Type : II

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PharmaCompass offers a list of Ectoine 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 Ectoine manufacturer or Ectoine supplier for your needs.
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PharmaCompass also assists you with knowing the Ectoine API Price utilized in the formulation of products. Ectoine API Price is not always fixed or binding as the Ectoine Price is obtained through a variety of data sources. The Ectoine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A CHEMBL1230264 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CHEMBL1230264, including repackagers and relabelers. The FDA regulates CHEMBL1230264 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CHEMBL1230264 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 CHEMBL1230264 supplier is an individual or a company that provides CHEMBL1230264 active pharmaceutical ingredient (API) or CHEMBL1230264 finished formulations upon request. The CHEMBL1230264 suppliers may include CHEMBL1230264 API manufacturers, exporters, distributors and traders.
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A CHEMBL1230264 DMF (Drug Master File) is a document detailing the whole manufacturing process of CHEMBL1230264 active pharmaceutical ingredient (API) in detail. Different forms of CHEMBL1230264 DMFs exist exist since differing nations have different regulations, such as CHEMBL1230264 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A CHEMBL1230264 DMF submitted to regulatory agencies in the US is known as a USDMF. CHEMBL1230264 USDMF includes data on CHEMBL1230264's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The CHEMBL1230264 USDMF is kept confidential to protect the manufacturer’s intellectual property.
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