Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
01 1Biophore India Pharmaceuticals Pvt Ltd
02 1LGM Pharma
03 1Rochem International Inc
04 1Supriya Lifescience
05 1Arde’s Laboratories
06 1Brother Enterprises Holding
07 1Divis Laboratories
08 1GE Healthcare Inc
09 1Global Calcium
10 1Grupo Juste
11 1Hengdian Group
12 1Hetero Drugs
13 1Hovione
14 1Interpharma Praha AS
15 1JRC
16 3ZHEJIANG TAIZHOU QINGQUAN MEDICAL & CHEM
17 1Zhejiang Haisen Pharmaceutical Co., Ltd.
18 2Zhejiang Starry Pharmaceutical Co., Ltd
01 8China
02 1Czech Republic
03 7India
04 1Portugal
05 1Spain
06 2U.S.A
07 1United Kingdom
01 2Active
02 3Inactive
03 16Blank
01 8Valid
02 1Withdrawn by Holder
03 12Blank
01 1217MF10959
02 1219MF10263
03 1227MF10106
04 1304MF10054
05 1305MF10075
06 1306MF10155
07 15Blank
01 21Blank
Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
Rochem, your partner in developing, sourcing, and supplying pharmaceutical & animal health ingredients of Chinese origin.
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
GDUFA
DMF Review : Reviewed
Rev. Date : 2023-05-03
Pay. Date : 2023-03-23
DMF Number : 38195
Submission : 2023-03-20
Status : Active
Type : II
Certificate Number : CEP 2022-240 - Rev 00
Issue Date : 2024-04-19
Type : Chemical
Substance Number : 1114
Status : Valid
NDC Package Code : 62331-066
Start Marketing Date : 2022-07-04
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Parmarine Co., Ltd.
Registration Date : 2022-05-17
Registration Number : 20220517-210-J-1297
Manufacturer Name : Divi's Laboratories Ltd.
Manufacturer Address : Unit-2, Chippada Village, Annavaram Post – 531 162, Bheemunipatnam Mandal, Visakhapatnam District, Andhra Pradesh, INDIA
GDUFA
DMF Review : Reviewed
Rev. Date : 2021-10-13
Pay. Date : 2021-09-14
DMF Number : 36038
Submission : 2021-09-15
Status : Active
Type : II
Certificate Number : R1-CEP 2009-018 - Rev 02
Issue Date : 2018-02-08
Type : Chemical
Substance Number : 1114
Status : Valid
NDC Package Code : 43228-100
Start Marketing Date : 1985-12-26
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Sangjin Corporation
Registration Date : 2024-12-24
Registration Number : 20210308-210-J-719(A)
Manufacturer Name : Zhejiang Starry Pharmaceutical Co., Ltd.
Manufacturer Address : No.1 Starry Road of Xianju Modern Industrial Centralization Zone, Xianju, Zhejiang, 317300, China
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 23148
Submission : 2009-10-02
Status : Inactive
Type : II
Certificate Number : R1-CEP 1999-044 - Rev 02
Issue Date : 2013-01-17
Type : Chemical
Substance Number : 1114
Status : Withdrawn by Holder
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 26641
Submission : 2013-01-24
Status : Inactive
Type : II
Certificate Number : R1-CEP 2000-018 - Rev 02
Issue Date : 2014-09-02
Type : Chemical
Substance Number : 1114
Status : Valid
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 22535
Submission : 2009-02-23
Status : Inactive
Type : II
Certificate Number : R0-CEP 2021-313 - Rev 00
Issue Date : 2022-03-02
Type : Chemical
Substance Number : 1114
Status : Valid
Registration Number : 304MF10054
Registrant's Address : No. 1 Starry Road of Xianju Modern Industrial Centralization Zone, Xianju, Zhejiang, 317300, China
Initial Date of Registration : 2022-03-16
Latest Date of Registration : --
NDC Package Code : 43228-100
Start Marketing Date : 1985-12-26
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Sangjin Corporation
Registration Date : 2024-12-24
Registration Number : 20210308-210-J-719(A)
Manufacturer Name : Zhejiang Starry Pharmaceutical Co., Ltd.
Manufacturer Address : No.1 Starry Road of Xianju Modern Industrial Centralization Zone, Xianju, Zhejiang, 317300, China
Certificate Number : R0-CEP 2020-098 - Rev 00
Issue Date : 2021-10-28
Type : Chemical
Substance Number : 1114
Status : Valid
Registration Number : 217MF10959
Registrant's Address : Lindesnesveien 208, 4521 Lindesnes, Norway
Initial Date of Registration : 2005-11-14
Latest Date of Registration : --
Registrant Name : Korea Biochem Pharmaceutical Co., Ltd.
Registration Date : 2020-07-17
Registration Number : 20200107-210-J-363(2)
Manufacturer Name : GE Healthcare AS
Manufacturer Address : Lindesnesveien 208, Lindesnes, NO-4521, Norway
Certificate Number : CEP 2022-221 - Rev 00
Issue Date : 2024-01-19
Type : Chemical
Substance Number : 1114
Status : Valid
Registration Number : 305MF10075
Registrant's Address : No. 01 Pengze Nine road, Jishan Industrial Park, Pengze County, Jiujiang City, Jiangxi Province, China
Initial Date of Registration : 2023-07-05
Latest Date of Registration : --
Registration Number : 227MF10106
Registrant's Address : Zhejiang Province Chemical and Medical Materials Base, Linhai Park
Initial Date of Registration : 2015-04-09
Latest Date of Registration : --
Certificate Number : R1-CEP 2014-098 - Rev 00
Issue Date : 2022-04-19
Type : Chemical
Substance Number : 1114
Status : Valid
Certificate Number : R1-CEP 2009-192 - Rev 02
Issue Date : 2020-05-20
Type : Chemical
Substance Number : 1114
Status : Valid
Registration Number : 219MF10263
Registrant's Address : Zhejiang Province Chemical and Medical Materials Base, Linhai Park
Initial Date of Registration : 2007-08-16
Latest Date of Registration : --
Registration Number : 306MF10155
Registrant's Address : Zhejiang Province Chemical and Medical Materials Base, Linhai Park
Initial Date of Registration : 2024-12-04
Latest Date of Registration : --
A Iohexol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Iohexol, including repackagers and relabelers. The FDA regulates Iohexol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Iohexol 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 Iohexol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Iohexol supplier is an individual or a company that provides Iohexol active pharmaceutical ingredient (API) or Iohexol finished formulations upon request. The Iohexol suppliers may include Iohexol API manufacturers, exporters, distributors and traders.
click here to find a list of Iohexol suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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