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01 1Alkermes Plc
02 1EASTMAN KODAK
03 1Novartis Pharmaceuticals Corporation
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01 1GLYCOLIDE
02 1MEDISORB
03 1POLY (DL-LACTIDE-CO-GLYCOLIDE)
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01 1Ireland
02 1Switzerland
03 1U.S.A
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01 2Active
02 1Inactive
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01 3Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 8481
Submission : 1990-03-15
Status : Active
Type : IV
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 1973
Submission : 1972-07-27
Status : Inactive
Type : IV
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 6895
Submission : 1987-03-26
Status : Active
Type : II
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PharmaCompass offers a list of Glycolide - lactide copolymer 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 Glycolide - lactide copolymer manufacturer or Glycolide - lactide copolymer supplier for your needs.
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PharmaCompass also assists you with knowing the Glycolide - lactide copolymer API Price utilized in the formulation of products. Glycolide - lactide copolymer API Price is not always fixed or binding as the Glycolide - lactide copolymer Price is obtained through a variety of data sources. The Glycolide - lactide copolymer Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Resomer RG 501H manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Resomer RG 501H, including repackagers and relabelers. The FDA regulates Resomer RG 501H manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Resomer RG 501H 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 Resomer RG 501H supplier is an individual or a company that provides Resomer RG 501H active pharmaceutical ingredient (API) or Resomer RG 501H finished formulations upon request. The Resomer RG 501H suppliers may include Resomer RG 501H API manufacturers, exporters, distributors and traders.
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A Resomer RG 501H DMF (Drug Master File) is a document detailing the whole manufacturing process of Resomer RG 501H active pharmaceutical ingredient (API) in detail. Different forms of Resomer RG 501H DMFs exist exist since differing nations have different regulations, such as Resomer RG 501H USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Resomer RG 501H DMF submitted to regulatory agencies in the US is known as a USDMF. Resomer RG 501H USDMF includes data on Resomer RG 501H's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Resomer RG 501H USDMF is kept confidential to protect the manufacturer’s intellectual property.
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