Bioiberica is a global life science company committed to improving the health & wellbeing of people, animals & plants.
01 3Bioiberica
02 1Sanofi
03 4Aspen API
04 1Pfizer CentreOne
05 1Akron Biotech
06 2Amphastar Pharmaceuticals
07 1Biocon
08 1Biofer
09 1CORLINE SYSTEMS AB
10 2Changzhou Qianhong
11 1Changzhou SPL Company, Ltd
12 1China Resources Zizhu Pharmaceutical
13 3DMFs Not Supported
14 1Dongying Tiandong Pharmaceutical Co., Ltd.
15 1F. Hoffmann-La Roche
16 8Fujifilm Diosynth Biotechnologies
17 1GLAND PHARMA LIMITED
18 2HEBEI CHANGSHAN BIOCHEMICAL PHARMACEUTICAL CO., LTD.
19 1HUAIAN MDC PHARMACEUTICAL CO.,LTD.
20 2Hubei Enoray Biopharmaceutical
21 3Laboratori Derivati Organici
22 2Laboratorio Syntex S.A
23 4Leo Pharma
24 1Medimpex
25 1Merck & Co
26 1Nanjing King-friend Biochemical Pharmaceutical
27 1Proquimes
28 1Sandoz B2B
29 3Scientific Protein Lab
30 1Shandong Chenzhong Biopharmaceutical Co.
31 1Shanghai NO 1 Biochemical & Pharmaceutical
32 1Shenzhen Hepalink Pharmaceutical
33 1Sichuan Deebio Pharmaceutical Co., Ltd
34 7Smithfield BioScience
35 1Weddel Limited
36 1Welding GmbH & Co.KG
37 1Yantai Dongcheng Biochemicals Co.,Ltd.
38 10Blank
Bioiberica is a global life science company committed to improving the health & wellbeing of people, animals & plants.
GDUFA
DMF Review : Complete
Rev. Date : 2013-05-09
Pay. Date : 2013-04-26
DMF Number : 17838
Submission : 2004-11-03
Status :
Type : II
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 9472
Submission : 1991-12-23
Status :
Type : II
Aspen API. More than just an API.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 5878
Submission : 1985-05-29
Status :
Type : II
Pfizer CentreOne is a global CDMO and a leading supplier of Specialty APIs.
GDUFA
DMF Review : Complete
Rev. Date : 2020-09-15
Pay. Date : 2020-09-14
DMF Number : 2712
Submission : 1976-08-03
Status :
Type : II
Bioiberica is a global life science company committed to improving the health & wellbeing of people, animals & plants.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 31738
Submission : 2017-05-17
Status :
Type : II
Bioiberica is a global life science company committed to improving the health & wellbeing of people, animals & plants.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 26680
Submission : 2013-01-07
Status :
Type : II
Aspen API. More than just an API.
GDUFA
DMF Review : Complete
Rev. Date : 2022-10-11
Pay. Date : 2022-08-16
DMF Number : 36291
Submission : 2021-09-22
Status :
Type : II
Aspen API. More than just an API.
GDUFA
DMF Review : Complete
Rev. Date : 2018-07-16
Pay. Date : 2018-06-28
DMF Number : 9131
Submission : 1991-05-09
Status :
Type : II
Aspen API. More than just an API.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 34686
Submission : 2020-03-17
Status :
Type : II
A Heparin Sodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Heparin Sodium, including repackagers and relabelers. The FDA regulates Heparin Sodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Heparin Sodium 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 Heparin Sodium manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Heparin Sodium supplier is an individual or a company that provides Heparin Sodium active pharmaceutical ingredient (API) or Heparin Sodium finished formulations upon request. The Heparin Sodium suppliers may include Heparin Sodium API manufacturers, exporters, distributors and traders.
click here to find a list of Heparin Sodium suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Heparin Sodium DMF (Drug Master File) is a document detailing the whole manufacturing process of Heparin Sodium active pharmaceutical ingredient (API) in detail. Different forms of Heparin Sodium DMFs exist exist since differing nations have different regulations, such as Heparin Sodium USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Heparin Sodium DMF submitted to regulatory agencies in the US is known as a USDMF. Heparin Sodium USDMF includes data on Heparin Sodium's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Heparin Sodium USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Heparin Sodium suppliers with USDMF on PharmaCompass.
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