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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PharmaCompass also assists you with knowing the Caninsulin API Price utilized in the formulation of products. Caninsulin API Price is not always fixed or binding as the Caninsulin Price is obtained through a variety of data sources. The Caninsulin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A SEMILENTE manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of SEMILENTE, including repackagers and relabelers. The FDA regulates SEMILENTE manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. SEMILENTE 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 SEMILENTE supplier is an individual or a company that provides SEMILENTE active pharmaceutical ingredient (API) or SEMILENTE finished formulations upon request. The SEMILENTE suppliers may include SEMILENTE API manufacturers, exporters, distributors and traders.
click here to find a list of SEMILENTE suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A SEMILENTE DMF (Drug Master File) is a document detailing the whole manufacturing process of SEMILENTE active pharmaceutical ingredient (API) in detail. Different forms of SEMILENTE DMFs exist exist since differing nations have different regulations, such as SEMILENTE USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A SEMILENTE DMF submitted to regulatory agencies in the US is known as a USDMF. SEMILENTE USDMF includes data on SEMILENTE's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The SEMILENTE USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of SEMILENTE suppliers with USDMF on PharmaCompass.
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