01 1Arcadia Lifescience
02 1Hebei Jiheng Pharmaceutical Co Ltd
03 1Hengdian Group
04 1Shandong Xinhua Pharmaceutical
05 1VANI PHARMA LABS LIMITED
06 1Wuhan Wuyao Pharmaceutical
07 1Yashiro Pharmaceutical Co Ltd
08 1Zhejiang Haisen Pharmaceutical Co., Ltd.
01 1Canada
02 5China
03 1India
04 1Blank
01 1Active
02 1Inactive
03 6Blank
01 4Valid
02 1Withdrawn by EDQM Failure to CEP procedure
03 3Blank
01 1222MF10084
02 1229MF10033
03 6Blank
01 8Blank
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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Status : Withdrawn by EDQM F...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 Analginum manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Analginum, including repackagers and relabelers. The FDA regulates Analginum manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Analginum 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 Analginum manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Analginum supplier is an individual or a company that provides Analginum active pharmaceutical ingredient (API) or Analginum finished formulations upon request. The Analginum suppliers may include Analginum API manufacturers, exporters, distributors and traders.
click here to find a list of Analginum suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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