01 1Eli Lilly
02 1Novo Nordisk
03 2Blank
01 1INSULIN USP(MONOCOMPONENT-MC)
02 1ZINC INSULIN CRYSTALS
03 1ZINC INSULIN CRYSTALS, INSULIN SALT CAKE (BULK)
04 1ZINC INSULIN CRYSTALS--ARGENTINA DMF-2912
01 1Denmark
02 1U.S.A
03 2Blank
01 4Inactive
01 4Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 2912
Submission : 1976-12-22
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3402
Submission : 1979-01-12
Status : Inactive
Type : II
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3967
Submission : 1980-10-23
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 : 2489
Submission : 1974-09-03
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
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PharmaCompass offers a list of Caninsulin 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 Caninsulin manufacturer or Caninsulin supplier for your needs.
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A Insulin novo lente manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Insulin novo lente, including repackagers and relabelers. The FDA regulates Insulin novo lente manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Insulin novo lente 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 Insulin novo lente supplier is an individual or a company that provides Insulin novo lente active pharmaceutical ingredient (API) or Insulin novo lente finished formulations upon request. The Insulin novo lente suppliers may include Insulin novo lente API manufacturers, exporters, distributors and traders.
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A Insulin novo lente DMF (Drug Master File) is a document detailing the whole manufacturing process of Insulin novo lente active pharmaceutical ingredient (API) in detail. Different forms of Insulin novo lente DMFs exist exist since differing nations have different regulations, such as Insulin novo lente USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Insulin novo lente DMF submitted to regulatory agencies in the US is known as a USDMF. Insulin novo lente USDMF includes data on Insulin novo lente's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Insulin novo lente USDMF is kept confidential to protect the manufacturer’s intellectual property.
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