EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
01 1EUROAPI
02 1Arcadia Lifescience
03 1Hebei Jiheng Pharmaceutical Co Ltd
04 1Hengdian Group
05 1Shandong Xinhua Pharmaceutical
06 1VANI PHARMA LABS LIMITED
07 1Wuhan Wuyao Pharmaceutical
08 1Yashiro Pharmaceutical Co Ltd
09 1Zhejiang Haisen Pharmaceutical Co., Ltd.
01 1Canada
02 5China
03 1France
04 1India
05 1Blank
01 1Active
02 1Inactive
03 7Blank
01 5Valid
02 1Withdrawn by EDQM Failure to CEP procedure
03 3Blank
01 1222MF10084
02 1229MF10033
03 7Blank
01 9Blank
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Certificate Number : R1-CEP 2000-277 - Rev 06
Issue Date : 2021-12-10
Type : Chemical
Substance Number : 1346
Status : Valid
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 31035
Submission : 2016-10-19
Status : Active
Type : II
Certificate Number : R1-CEP 2001-356 - Rev 04
Issue Date : 2017-08-11
Type : Chemical
Substance Number : 1346
Status : Valid
NDC Package Code : 58624-0707
Start Marketing Date : 2024-03-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 17006
Submission : 2003-12-08
Status : Inactive
Type : II
Certificate Number : R1-CEP 2005-143 - Rev 02
Issue Date : 2021-03-03
Type : Chemical
Substance Number : 1346
Status : Valid
NDC Package Code : 81919-005
Start Marketing Date : 2020-10-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Certificate Number : R1-CEP 2001-220 - Rev 01
Issue Date : 2008-09-08
Type : Chemical
Substance Number : 1346
Status : Withdrawn by EDQM F...
Certificate Number : R1-CEP 2004-016 - Rev 03
Issue Date : 2021-07-28
Type : Chemical
Substance Number : 1346
Status : Valid
Certificate Number : CEP 2014-091 - Rev 02
Issue Date : 2024-07-31
Type : Chemical
Substance Number : 1346
Status : Valid
Registration Number : 229MF10033
Registrant's Address : Room No. 1-6, Floor 23, Building 1#, No. 160 Qiaokou Road Qiaokou District
Initial Date of Registration : 2017-02-08
Latest Date of Registration :
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
Registration Number : 222MF10084
Registrant's Address : 10-2 Yoshida Shimojima, Higashiosaka City, Osaka Prefecture
Initial Date of Registration : 2010-03-16
Latest Date of Registration :
A Novaminsulfon manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Novaminsulfon, including repackagers and relabelers. The FDA regulates Novaminsulfon manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Novaminsulfon 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 Novaminsulfon manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Novaminsulfon supplier is an individual or a company that provides Novaminsulfon active pharmaceutical ingredient (API) or Novaminsulfon finished formulations upon request. The Novaminsulfon suppliers may include Novaminsulfon API manufacturers, exporters, distributors and traders.
click here to find a list of Novaminsulfon suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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