Rochem, your partner in developing, sourcing, and supplying pharmaceutical & animal health ingredients of Chinese origin.

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01 1Rochem International Inc
02 1Tenatra Exports
03 1Calao s.r.l. IT 20157 Milano
04 1Cambrex Corporation
05 1Chugoku Kayaku
06 1Curia
07 1DOTTIKON EXCLUSIVE SYNTHESIS AG
08 3Dipharma
09 1EIRCHEM Pharma Services
10 1IQT Industrias Quimicas Taubate
11 1JP Laboratories
12 1Kremers Urban Pharmaceuticals
13 4Lunan Pharmaceutical
14 1Muromachi Chemicals Inc
15 1NORDIC SYNTHESIS AB
16 1RA CHEM PHARMA LIMITED
17 3Shandong Keyuan Pharmaceutical
18 1WHYTE CHEMICALS
19 1Zhuhai Rundu Pharmaceutical
20 1Zim Laboratories
21 2Blank
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01 1Brazil
02 8China
03 4India
04 1Ireland
05 3Italy
06 2Japan
07 1Sweden
08 1Switzerland
09 5U.S.A
10 1United Kingdom
11 2Blank
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01 5Active
02 7Inactive
03 17Blank
01 6Valid
02 3Withdrawn by EDQM Failure to CEP procedure
03 1Withdrawn by Holder
04 19Blank
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01 1217MF10798
02 1218MF10745
03 1225MF10192
04 1229MF10189
05 25Blank
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01 1WC-0106
02 28Blank
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01 120210325-209-J-775
02 120211129-209-J-654
03 120220324-209-J-1239
04 120220324-209-J-1239(1)
05 120220504-209-J-1260
06 24Blank
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01 142677-101
02 142677-102
03 146438-0025
04 146438-0027
05 146438-1110
06 24Blank
01 29Blank
Rochem, your partner in developing, sourcing, and supplying pharmaceutical & animal health ingredients of Chinese origin.
Tenatra connects Indian manufacturers with global buyers through active partners in Germany, Switzerland, Belgium, Spain & Turkey.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 6362
Submission : 1984-10-04
Status : Active
Type : II

GDUFA
DMF Review : Reviewed
Rev. Date : 2013-01-15
Pay. Date : 2012-12-24
DMF Number : 6778
Submission : 1987-01-09
Status : Active
Type : II
Certificate Number : R1-CEP 2007-261 - Rev 02
Issue Date : 2021-12-01
Type : Chemical
Substance Number : 1118
Status : Valid
Registration Number : 218MF10745
Registrant's Address : Via Bissone, 5, 20021-Baranzate, Milano, Italy
Initial Date of Registration : 2006-09-06
Latest Date of Registration :
NDC Package Code : 46438-1110
Start Marketing Date : 2014-05-26
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Samoh Pharmaceutical Co., Ltd.
Registration Date : 2022-05-04
Registration Number : 20220504-209-J-1260
Manufacturer Name : Dipharma Francis Srl
Manufacturer Address : Via XXIV Maggio 40-33036 Mereto di Tomba (UD) Italy

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 5607
Submission : 1984-11-15
Status : Inactive
Type : II

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 21809
Submission : 2008-06-18
Status : Inactive
Type : II
Certificate Number : CEP 2008-112 - Rev 01
Issue Date : 2024-04-10
Type : Chemical
Substance Number : 1118
Status : Valid
Registration Number : 229MF10189
Registrant's Address : Keyuan Street, Shandong Shanghe Economic Development Zone, Jinan City, Shandong, China
Initial Date of Registration : 2017-10-26
Latest Date of Registration :
Registrant Name : Hyundai Pharmaceutical Co., Ltd.
Registration Date : 2022-04-05
Registration Number : 20220324-209-J-1239(1)
Manufacturer Name : Shandong Keyuan Pharmaceutical Co., Ltd.
Manufacturer Address : Keyuan Street, Shandong Shanghe Economic Development Zone, Jinan, Shandong, China

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 : 6777
Submission : 1987-01-09
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 : 6803
Submission : 1987-02-05
Status : Inactive
Type : II

Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 6789
Submission : 1987-01-23
Status : Inactive
Type : II

Certificate Number : R1-CEP 2006-299 - Rev 04
Issue Date : 2022-08-30
Type : Chemical
Substance Number : 1118
Status : Valid

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A Monicor manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Monicor, including repackagers and relabelers. The FDA regulates Monicor manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Monicor API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Monicor supplier is an individual or a company that provides Monicor active pharmaceutical ingredient (API) or Monicor finished formulations upon request. The Monicor suppliers may include Monicor API manufacturers, exporters, distributors and traders.
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We have 20 companies offering Monicor
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