01 1SALSBURY CHEMICALS INC
02 1Siegfried AG
03 3Blank
01 1FRAMYCETIN (SOFROMYCIN ROUSSEL)
02 1NEODECYLLIN (NEOMYCIN UNDECYLENATE)
03 1NEOMYCIN BASE - MF'G PROCEDURES & SPECS
04 1TYLOSIN & NEOMYCIN USED AS AN EXPERIMENTAL PRODUCT (VET)
05 1TYLOSIN 20MG PER CC AND NEOMYCIN 10MG PER CC (VET)
01 1Switzerland
02 1U.S.A
03 3Blank
01 5Inactive
01 5Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 292
Submission : 1940-01-01
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 406
Submission : 1960-11-07
Status : Inactive
Type : II
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 681
Submission : 1963-08-26
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 649
Submission : 1963-08-26
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 356
Submission : 1959-12-17
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
89
PharmaCompass offers a list of Neomycin 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 Neomycin manufacturer or Neomycin supplier for your needs.
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A Sofra-Tulle manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sofra-Tulle, including repackagers and relabelers. The FDA regulates Sofra-Tulle manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sofra-Tulle 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 Sofra-Tulle supplier is an individual or a company that provides Sofra-Tulle active pharmaceutical ingredient (API) or Sofra-Tulle finished formulations upon request. The Sofra-Tulle suppliers may include Sofra-Tulle API manufacturers, exporters, distributors and traders.
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A Sofra-Tulle DMF (Drug Master File) is a document detailing the whole manufacturing process of Sofra-Tulle active pharmaceutical ingredient (API) in detail. Different forms of Sofra-Tulle DMFs exist exist since differing nations have different regulations, such as Sofra-Tulle USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Sofra-Tulle DMF submitted to regulatory agencies in the US is known as a USDMF. Sofra-Tulle USDMF includes data on Sofra-Tulle's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Sofra-Tulle USDMF is kept confidential to protect the manufacturer’s intellectual property.
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