01 4Fujifilm Diosynth Biotechnologies
02 1Laboratorios Beta S.A. AR C1232 AAR Buenos Aires
03 3Novo Nordisk
04 1SIGMA TAU
01 1Argentina
02 3Denmark
03 1U.S.A
04 4United Kingdom
01 5Inactive
02 4Blank
01 1Valid
02 3Withdrawn by Holder
03 5Blank
01 9Blank
01 9Blank
01 9Blank
01 9Blank
01 9Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 7679
Submission : 1988-09-15
Status : Inactive
Type : II
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3865
Submission : 1980-06-19
Status : Inactive
Type : II
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3881
Submission : 1980-06-30
Status : Inactive
Type : II
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 14382
Submission : 1999-09-02
Status : Inactive
Type : II
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 14833
Submission : 2000-04-14
Status : Inactive
Type : II
Certificate Number : R0-CEP 2000-135 - Rev 02
Issue Date : 2005-03-08
Type : TSE
Substance Number :
Status : Withdrawn by Holder
Certificate Number : R0-CEP 2000-340 - Rev 02
Issue Date : 2005-03-08
Type : TSE
Substance Number :
Status : Withdrawn by Holder
Certificate Number : R1-CEP 2000-230 - Rev 00
Issue Date : 2006-05-17
Type : TSE
Substance Number :
Status : Withdrawn by Holder
Certificate Number : R1-CEP 2005-214 - Rev 00
Issue Date : 2011-01-07
Type : TSE
Substance Number :
Status : Valid
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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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.
We have 4 companies offering HUMULIN R PEN
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