Centrient is a leading manufacturer of Beta-Lactam Antibiotics and a provider of next-generation Statins and Antifungals.
01 1Centrient Pharmaceuticals
02 1LGM Pharma
03 1Suanfarma
04 1DKSH
05 1Jai Radhe Sales
06 1Atman Pharmaceuticals
07 2Bajaj Healthcare
08 1CHEMO
09 1Chemo Biosynthesis
10 1Dalian Richon Chem
11 1Delta Synthetic Co. Ltd
12 1Diligent Life Care
13 1Hangzhou Think Chemical Co.Ltd
14 2Hebei Veyong Pharmaceutical
15 2Hengdian Group
16 2Hovione
17 1Industriale Chimica
18 1Merck & Co
19 1North China Pharmaceutical Co., Ltd.
20 1RICHBERYL BIOTECH CO., LTD. OF RAOYANG COUNTY
21 1SAMEX OVERSEAS
22 1Shandong Qilu King-Phar Pharmaceutical Co., Ltd
23 1Sinobright Pharmaceutical Company Ltd
24 1Tecoland Corporation
25 1Xian Tian Guangyuan Biotech
26 1Zhejiang Apeloa Kangyu Pharmaceutical Co. Ltd
27 1Zhejiang Hisun Pharmaceutical
28 3Blank
01 13China
02 6India
03 2Italy
04 1Netherlands
05 2Portugal
06 2Spain
07 1Switzerland
08 1Taiwan
09 3U.S.A
10 3Blank
01 4Active
02 3Inactive
03 27Blank
01 2Expired
02 7Valid
03 1Withdrawn by Holder
04 24Blank
01 1221MF10281
02 1304MF10006
03 1304MF10048
04 31Blank
01 34Blank
Centrient is a leading manufacturer of Beta-Lactam Antibiotics and a provider of next-generation Statins and Antifungals.
LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-01-09
Pay. Date : 2012-12-14
DMF Number : 21395
Submission : 2008-03-05
Status : Active
Type : II
Certificate Number : R1-CEP 1998-138 - Rev 05
Issue Date : 2020-02-28
Type : Chemical
Substance Number : 1336
Status : Valid
Registration Number : 304MF10006
Registrant's Address : Estrada Coronel Nicolau de Mesquita Taipa, Macau S. A. R. China
Initial Date of Registration : 2022-01-11
Latest Date of Registration : --
NDC Package Code : 55018-121
Start Marketing Date : 1998-07-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2022-04-06
Pay. Date : 2022-01-13
DMF Number : 36494
Submission : 2021-11-15
Status : Active
Type : II
GDUFA
DMF Review : Reviewed
Rev. Date : 2014-02-08
Pay. Date : 2012-12-18
DMF Number : 21624
Submission : 2008-05-08
Status : Active
Type : II
Certificate Number : R1-CEP 1999-176 - Rev 05
Issue Date : 2021-03-31
Type : Chemical
Substance Number : 1336
Status : Valid
Registration Number : 304MF10048
Registrant's Address : 46 Waisha Road, Jiaojiang District, Taizhou City, Zhejiang Province, P. R. China 318000
Initial Date of Registration : 2022-03-02
Latest Date of Registration : --
NDC Package Code : 58623-0047
Start Marketing Date : 2014-10-24
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
VMF Number : 5553
Submission : 1995-12-14
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 17673
Submission : 2004-07-18
Status : Inactive
Type : II
Certificate Number : R0-CEP 2021-477 - Rev 00
Issue Date : 2022-04-22
Type : Chemical
Substance Number : 1336
Status : Valid
NDC Package Code : 49885-0006
Start Marketing Date : 2019-09-13
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
VMF Number : 5906
Submission : 2007-09-20
Status : Inactive
Type : II
Certificate Number : R1-CEP 2008-104 - Rev 02
Issue Date : 2020-06-08
Type : Chemical
Substance Number : 1336
Status : Withdrawn by Holder
NDC Package Code : 49885-0006
Start Marketing Date : 2019-09-13
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
VMF Number : 5906
Submission : 2007-09-20
Status : Inactive
Type : II
Certificate Number : R1-CEP 2004-070 - Rev 01
Issue Date : 2011-08-02
Type : Chemical
Substance Number : 1336
Status : Valid
NDC Package Code : 68171-0001
Start Marketing Date : 2007-12-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
VMF Number : 5774
Submission : 2003-06-10
Status : Active
Type : II
Certificate Number : R0-CEP 2010-123 - Rev 00
Issue Date : 2011-10-25
Type : Chemical
Substance Number : 1336
Status : Expired
Certificate Number : R0-CEP 2006-008 - Rev 01
Issue Date : 2010-06-17
Type : Chemical
Substance Number : 1336
Status : Expired
VMF Number : 5797
Submission : 2004-03-24
Status : Inactive
Type : II
Certificate Number : R1-CEP 2001-146 - Rev 01
Issue Date : 2008-11-27
Type : Chemical
Substance Number : 1336
Status : Valid
VMF Number : 5476
Submission : 1993-10-22
Status : Inactive
Type : II
Certificate Number : R1-CEP 2001-077 - Rev 01
Issue Date : 2017-10-16
Type : Chemical
Substance Number : 1336
Status : Valid
NDC Package Code : 66405-0001
Start Marketing Date : 2004-02-18
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
VMF Number : 5720
Submission : 2001-05-11
Status : Active
Type : II
Certificate Number : CEP 2021-382 - Rev 00
Issue Date : 2024-08-02
Type : Chemical
Substance Number : 1336
Status : Valid
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 : 38553
Submission : 2023-06-27
Status : Active
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
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 : 12755
Submission : 1997-11-21
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
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 : 13037
Submission : 1998-06-15
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
A Ivermectin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ivermectin, including repackagers and relabelers. The FDA regulates Ivermectin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ivermectin 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 Ivermectin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ivermectin supplier is an individual or a company that provides Ivermectin active pharmaceutical ingredient (API) or Ivermectin finished formulations upon request. The Ivermectin suppliers may include Ivermectin API manufacturers, exporters, distributors and traders.
click here to find a list of Ivermectin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
We have 27 companies offering Ivermectin
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?