Pfizer CentreOne is a global CDMO and a leading supplier of Specialty APIs.
01 1Pfizer CentreOne
02 1F.I.S. Fabbrica Italiana Sintetici
03 2Fujifilm Diosynth Biotechnologies
04 1Jiangsu Jiaerke Pharmaceuticals Group
05 2Merck & Co
06 2SIGMA TAU
07 1Zhejiang Xianju Junye Pharmaceutical Co. LTD
01 1DEHYDRO ISOANDROSTERONE
02 1DEHYDRO ISOANDROSTERONE ACETATE
03 1DEHYDROISOANDROSTERONE
04 1DEHYDROISOANDROSTERONE POLYMORPH I
05 1DEHYDROISOANDROSTERONE-3-SULFATE,SODIUM SALT
06 1DEHYROISOANDROSTERONE
07 4PRASTERONE ACETATE
01 2China
02 1Italy
03 5U.S.A
04 2United Kingdom
01 4Active
02 6Inactive
01 10Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 28729
Submission : 2014-12-11
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 27340
Submission : 2013-09-20
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 7535
Submission : 1988-06-13
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 7524
Submission : 1988-06-13
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 24438
Submission : 2010-12-10
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 14283
Submission : 1999-07-12
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 10691
Submission : 1994-01-24
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 5119
Submission : 1983-09-20
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3958
Submission : 1980-10-08
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 28254
Submission : 2014-04-25
Status : Active
Type : II
A CAS-853-23-6 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CAS-853-23-6, including repackagers and relabelers. The FDA regulates CAS-853-23-6 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CAS-853-23-6 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of CAS-853-23-6 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A CAS-853-23-6 supplier is an individual or a company that provides CAS-853-23-6 active pharmaceutical ingredient (API) or CAS-853-23-6 finished formulations upon request. The CAS-853-23-6 suppliers may include CAS-853-23-6 API manufacturers, exporters, distributors and traders.
click here to find a list of CAS-853-23-6 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A CAS-853-23-6 DMF (Drug Master File) is a document detailing the whole manufacturing process of CAS-853-23-6 active pharmaceutical ingredient (API) in detail. Different forms of CAS-853-23-6 DMFs exist exist since differing nations have different regulations, such as CAS-853-23-6 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A CAS-853-23-6 DMF submitted to regulatory agencies in the US is known as a USDMF. CAS-853-23-6 USDMF includes data on CAS-853-23-6's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The CAS-853-23-6 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of CAS-853-23-6 suppliers with USDMF on PharmaCompass.
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