Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
01 3Sanofi
01 1IGEPAL CA 630 SPECIAL (OCTOXYNOL-9)
02 1IGEPAL CA-630G (OCTOXYNOL 9)
03 1IGEPAL CO 887 (SAME AS IGEPAL 880) CONTRLS & TOXICITY
01 3France
01 3Inactive
01 3Blank
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 404
Submission : 1960-10-27
Status : Inactive
Type : II
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 12303
Submission : 1996-12-16
Status : Inactive
Type : II
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 6266
Submission : 1986-04-11
Status : Inactive
Type : II
90
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A Triton X 705 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Triton X 705, including repackagers and relabelers. The FDA regulates Triton X 705 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Triton X 705 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Triton X 705 supplier is an individual or a company that provides Triton X 705 active pharmaceutical ingredient (API) or Triton X 705 finished formulations upon request. The Triton X 705 suppliers may include Triton X 705 API manufacturers, exporters, distributors and traders.
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A Triton X 705 DMF (Drug Master File) is a document detailing the whole manufacturing process of Triton X 705 active pharmaceutical ingredient (API) in detail. Different forms of Triton X 705 DMFs exist exist since differing nations have different regulations, such as Triton X 705 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Triton X 705 DMF submitted to regulatory agencies in the US is known as a USDMF. Triton X 705 USDMF includes data on Triton X 705's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Triton X 705 USDMF is kept confidential to protect the manufacturer’s intellectual property.
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