01 1Abbott Laboratories
01 1SPECTINOMYCIN (M-141, ABBOTT) (VET)
01 1U.S.A
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 628
Submission : 1963-08-08
Status : Inactive
Type : II
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A Togamycin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Togamycin, including repackagers and relabelers. The FDA regulates Togamycin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Togamycin 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 Togamycin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Togamycin supplier is an individual or a company that provides Togamycin active pharmaceutical ingredient (API) or Togamycin finished formulations upon request. The Togamycin suppliers may include Togamycin API manufacturers, exporters, distributors and traders.
click here to find a list of Togamycin suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Togamycin DMF (Drug Master File) is a document detailing the whole manufacturing process of Togamycin active pharmaceutical ingredient (API) in detail. Different forms of Togamycin DMFs exist exist since differing nations have different regulations, such as Togamycin USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Togamycin DMF submitted to regulatory agencies in the US is known as a USDMF. Togamycin USDMF includes data on Togamycin's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Togamycin USDMF is kept confidential to protect the manufacturer’s intellectual property.
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