Century has been an API manufacturer for over 40 years & is the partner of choice for multipurpose custom manufacturing projects.
01 1Century Pharmaceuticals
02 1AbbVie Inc
03 2Abbott Laboratories
04 1Alembic Pharmaceuticals Limited
05 1Archimica
06 1Ercros
07 1Fermic
08 1SM BIOMED
09 1Sandoz B2B
10 1Solara Active Pharma Sciences
Century has been an API manufacturer for over 40 years & is the partner of choice for multipurpose custom manufacturing projects.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 34581
Submission : 2020-03-09
Status :
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13443
Submission : 1998-09-01
Status :
Type : II
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PharmaCompass offers a list of Erythromycin Ethyl Succinate 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 Erythromycin Ethyl Succinate manufacturer or Erythromycin Ethyl Succinate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Erythromycin Ethyl Succinate manufacturer or Erythromycin Ethyl Succinate supplier.
PharmaCompass also assists you with knowing the Erythromycin Ethyl Succinate API Price utilized in the formulation of products. Erythromycin Ethyl Succinate API Price is not always fixed or binding as the Erythromycin Ethyl Succinate Price is obtained through a variety of data sources. The Erythromycin Ethyl Succinate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 1264-62-6 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 1264-62-6, including repackagers and relabelers. The FDA regulates 1264-62-6 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 1264-62-6 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 1264-62-6 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A 1264-62-6 supplier is an individual or a company that provides 1264-62-6 active pharmaceutical ingredient (API) or 1264-62-6 finished formulations upon request. The 1264-62-6 suppliers may include 1264-62-6 API manufacturers, exporters, distributors and traders.
click here to find a list of 1264-62-6 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A 1264-62-6 DMF (Drug Master File) is a document detailing the whole manufacturing process of 1264-62-6 active pharmaceutical ingredient (API) in detail. Different forms of 1264-62-6 DMFs exist exist since differing nations have different regulations, such as 1264-62-6 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A 1264-62-6 DMF submitted to regulatory agencies in the US is known as a USDMF. 1264-62-6 USDMF includes data on 1264-62-6's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The 1264-62-6 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of 1264-62-6 suppliers with USDMF on PharmaCompass.
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