01 1Akums Lifesciences
02 2Aurobindo Pharma Limited
03 1Covalent Laboratories Private Limited
04 2Daiichi Sankyo
05 1Nectar Lifesciences
06 1Orchid Pharma
07 1Qilu Antibiotics Pharmaceutical Co., Ltd.
08 1RANBAXY LABORATORIES LIMITED
09 2Sandoz B2B
01 4CEFPODOXIME PROXETIL
02 4CEFPODOXIME PROXETIL USP
03 1CEFPODOXIME PROXETIL USP (NON-STERILE BULK)
04 1CEFPODOXIME PROXETIL USP (PROCESS II)
05 1CS-807 CEFPODOXIME PROXETIL DRUG SUBSTANCE
06 1CS-807 TABLETS
01 1China
02 7India
03 2Japan
04 2Switzerland
01 8Active
02 4Inactive
01 4Complete
02 8Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 23572
Submission : 2010-02-23
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 18941
Submission : 2005-10-31
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2024-05-09
Pay. Date : 2024-03-21
DMF Number : 39541
Submission : 2024-03-27
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2017-02-27
Pay. Date : 2016-12-27
DMF Number : 29791
Submission : 2015-09-14
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 9886
Submission : 1987-04-15
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 6937
Submission : 1987-04-15
Status : Inactive
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2014-11-11
Pay. Date : 2014-06-18
DMF Number : 27071
Submission : 2014-06-14
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 18505
Submission : 2005-07-11
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2020-03-09
Pay. Date : 2020-01-21
DMF Number : 34502
Submission : 2020-02-17
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 20076
Submission : 2006-12-26
Status : Active
Type : II
A CAS-87239-81-4 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CAS-87239-81-4, including repackagers and relabelers. The FDA regulates CAS-87239-81-4 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CAS-87239-81-4 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A CAS-87239-81-4 supplier is an individual or a company that provides CAS-87239-81-4 active pharmaceutical ingredient (API) or CAS-87239-81-4 finished formulations upon request. The CAS-87239-81-4 suppliers may include CAS-87239-81-4 API manufacturers, exporters, distributors and traders.
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A CAS-87239-81-4 DMF (Drug Master File) is a document detailing the whole manufacturing process of CAS-87239-81-4 active pharmaceutical ingredient (API) in detail. Different forms of CAS-87239-81-4 DMFs exist exist since differing nations have different regulations, such as CAS-87239-81-4 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A CAS-87239-81-4 DMF submitted to regulatory agencies in the US is known as a USDMF. CAS-87239-81-4 USDMF includes data on CAS-87239-81-4's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The CAS-87239-81-4 USDMF is kept confidential to protect the manufacturer’s intellectual property.
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