01 1Avid Bioservices
02 1BBI Solutions
03 1Bioindustria L.I.M. Spa
04 1Catalent Pharma Solutions
05 1Fujifilm Diosynth Biotechnologies
06 1Reliable Biopharmaceutical Corporation
07 1SAFC
08 1SERAVAC BIOTECH PTY LTD
09 1SIGMA TAU
10 1Sichuan Deebio Pharmaceutical Co., Ltd
11 1Worthington Biochemical Corporation US 08701 Lakewood
01 1China
02 1Italy
03 1South Africa
04 6U.S.A
05 2United Kingdom
01 6Inactive
02 5Blank
01 1Expired
02 1Suspended by EDQM GMP non-compliance
03 1Valid
04 8Blank
01 1302MF10030
02 1304MF10126
03 9Blank
01 11Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3405
Submission : 1979-01-09
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 16273
Submission : 2002-11-25
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 : 4489
Submission : 1982-02-02
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 16622
Submission : 2003-05-30
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 26086
Submission : 2012-05-24
Status : Inactive
Type : II
Certificate Number : R0-CEP 2001-364 - Rev 01
Issue Date : 2005-03-18
Type : TSE
Substance Number : 912
Status : Expired
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 90
Submission : 1954-03-04
Status : Inactive
Type : II
Certificate Number : R1-CEP 2001-085 - Rev 02
Issue Date : 2010-06-01
Type : TSE
Substance Number : 912
Status : Valid
Registration Number : 304MF10126
Registrant's Address : 14191 Myford Road Tustin, CA 92780, USA
Initial Date of Registration : 2022-08-24
Latest Date of Registration : --
Registration Number : 302MF10030
Registrant's Address : 1300 South Patterson Drive, Bloomington, Indiana 47403 USA
Initial Date of Registration : 2020-02-20
Latest Date of Registration : --
Certificate Number : R1-CEP 2001-068 - Rev 00
Issue Date : 2007-04-04
Type : TSE
Substance Number : 912
Status : Suspended by EDQM G...
A Hyaluronidase manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Hyaluronidase, including repackagers and relabelers. The FDA regulates Hyaluronidase manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Hyaluronidase 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 Hyaluronidase manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Hyaluronidase supplier is an individual or a company that provides Hyaluronidase active pharmaceutical ingredient (API) or Hyaluronidase finished formulations upon request. The Hyaluronidase suppliers may include Hyaluronidase API manufacturers, exporters, distributors and traders.
click here to find a list of Hyaluronidase suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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