01 4Fujifilm Diosynth Biotechnologies
02 1SAFC
03 1SIGMA TAU
01 1BOVINE INSULIN
02 2BOVINE INSULIN HIGHLY PURIFIED
03 1BOVINE INSULINE HIGHLY PURIFIED
04 1INSULIN FROM BOVINE PANCREAS
05 1TrypZean Bovine, Recombinant Expressed in Corn
01 2U.S.A
02 4United Kingdom
01 6Inactive
01 6Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3881
Submission : 1980-06-30
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3865
Submission : 1980-06-19
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 14833
Submission : 2000-04-14
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 14382
Submission : 1999-09-02
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 21228
Submission : 2008-01-11
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 7679
Submission : 1988-09-15
Status : Inactive
Type : II
27
PharmaCompass offers a list of Bovine Insulin 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 Bovine Insulin manufacturer or Bovine Insulin supplier for your needs.
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PharmaCompass also assists you with knowing the Bovine Insulin API Price utilized in the formulation of products. Bovine Insulin API Price is not always fixed or binding as the Bovine Insulin Price is obtained through a variety of data sources. The Bovine Insulin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A HUMULIN R PEN manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of HUMULIN R PEN, including repackagers and relabelers. The FDA regulates HUMULIN R PEN manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. HUMULIN R PEN 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 HUMULIN R PEN supplier is an individual or a company that provides HUMULIN R PEN active pharmaceutical ingredient (API) or HUMULIN R PEN finished formulations upon request. The HUMULIN R PEN suppliers may include HUMULIN R PEN API manufacturers, exporters, distributors and traders.
click here to find a list of HUMULIN R PEN suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A HUMULIN R PEN DMF (Drug Master File) is a document detailing the whole manufacturing process of HUMULIN R PEN active pharmaceutical ingredient (API) in detail. Different forms of HUMULIN R PEN DMFs exist exist since differing nations have different regulations, such as HUMULIN R PEN USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A HUMULIN R PEN DMF submitted to regulatory agencies in the US is known as a USDMF. HUMULIN R PEN USDMF includes data on HUMULIN R PEN's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The HUMULIN R PEN USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of HUMULIN R PEN suppliers with USDMF on PharmaCompass.
We have 3 companies offering HUMULIN R PEN
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