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01 5Axplora
02 2Zhejiang Hengkang Pharmaceutical
03 15PharmaZell
04 1LGM Pharma
05 1Metrochem API Private Limited
06 1IOL Chemicals and Pharmaceuticals
07 1Jai Radhe Sales
08 1HRV Pharma
09 1Maithri Drugs
10 1Bayer AG
11 2A.H.A International
12 1ALP Pharm
13 1Ajinomoto Company
14 1Ajinomoto OmniChem N.V.
15 1Alkem Laboratories
16 1Alvogen
17 1Amoli Organics
18 1Anwita Drugs
19 1Aspire Lifesciences Pvt Ltd
20 1Aurobindo Pharma Limited
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23 2Cambrex Corporation
24 4Chemi SpA
25 1Cilag AG
26 2Corden Pharma Bergamo S.p.A
27 1Credo Life Sciences
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01 1219MF10036
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GDUFA
DMF Review : Reviewed
Rev. Date : 2014-12-16
Pay. Date : 2014-11-28
DMF Number : 8070
Submission : 1989-05-09
Status : Active
Type : II
Certificate Number : CEP 2003-203 - Rev 03
Issue Date : 2023-11-08
Type : Chemical
Substance Number : 1699
Status : Valid
Registration Number : 219MF10036
Registrant's Address : ROSENHEIMER STR. 43 D-83064 RAUBLING, Germany
Initial Date of Registration : 2007-02-13
Latest Date of Registration :
Registrant Name : Takeda Pharmaceutical Korea
Registration Date : 2021-10-05
Registration Number : 20210521-209-J-766(1)
Manufacturer Name : PharmaZell (India) Private Ltd
Manufacturer Address : Plot No. 115, Visakha Pharmacity Limited, SEZ, Parawada, Anakapalli – 531019 Andhra Pradesh, India
| Available Reg Filing : EU, CA, TW, BR, TH |
Zhejiang Hengkang Pharm Group is a dynamic pharmaceutical entity, spanning drug research, large-scale production, and global marketing.
GDUFA
DMF Review : Reviewed
Rev. Date : 2022-10-20
Pay. Date : 2022-09-16
DMF Number : 37319
Submission : 2022-08-17
Status : Active
Type : II
Certificate Number : CEP 2021-400 - Rev 01
Issue Date : 2025-12-10
Type : Chemical
Substance Number : 1699
Status : Valid
Registration Number : 305MF10102
Registrant's Address : No. 11 Chengen Road, Pubagan Town, Sanmen, Zhejiang, China
Initial Date of Registration : 2023-08-30
Latest Date of Registration :
Date of Issue : 2022-04-28
Valid Till : 2024-12-15
Written Confirmation Number : ZJ220039
Address of the Firm :
Registrant Name : Huseong Bio Co., Ltd.
Registration Date : 2026-04-23
Registration Number : 20260423-209-J-2466
Manufacturer Name : Zhejiang Hengkang Pharmaceutical Co., Ltd.
Manufacturer Address : No. 11 Chengen Road, Pubagang Town, Sanmen, Zhejiang, China
| Available Reg Filing : BR |
NDC Package Code : 12598-9154
Start Marketing Date : 2021-10-09
End Marketing Date : 2027-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
Metrochem has been delivering customized volume & quality products to customers across the world, taking utmost care of their needs.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 38338
Submission : 2023-10-14
Status : Active
Type : II
Certificate Number : CEP 2023-339 - Rev 00
Issue Date : 2025-01-16
Type : Chemical
Substance Number : 1699
Status : Valid
NDC Package Code : 49716-337
Start Marketing Date : 2023-10-25
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 31570
Submission : 2017-03-31
Status : Active
Type : II
Certificate Number : R1-CEP 2017-116 - Rev 00
Issue Date : 2023-04-13
Type : Chemical
Substance Number : 1699
Status : Valid
Date of Issue : 2024-02-12
Valid Till : 2027-02-11
Written Confirmation Number : WC-0407
Address of the Firm :
NDC Package Code : 70600-006
Start Marketing Date : 2021-12-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
| Available Reg Filing : ASMF, BR |
Bayer AG manufactures innovative APIs and pharmaceutical formulations across diverse therapeutic areas.
Registration Number : 224MF10001
Registrant's Address : 13353 Berlin, Muellerstrasse 178, Germany
Initial Date of Registration : 2012-01-16
Latest Date of Registration :
NDC Package Code : 12527-1721
Start Marketing Date : 2013-04-15
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Mesalazine API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Mesalazine manufacturer or Mesalazine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Mesalazine manufacturer or Mesalazine supplier.
A 35589-28-7 (mono-hydrochloride salt) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 35589-28-7 (mono-hydrochloride salt), including repackagers and relabelers. The FDA regulates 35589-28-7 (mono-hydrochloride salt) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 35589-28-7 (mono-hydrochloride salt) 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 35589-28-7 (mono-hydrochloride salt) manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A 35589-28-7 (mono-hydrochloride salt) supplier is an individual or a company that provides 35589-28-7 (mono-hydrochloride salt) active pharmaceutical ingredient (API) or 35589-28-7 (mono-hydrochloride salt) finished formulations upon request. The 35589-28-7 (mono-hydrochloride salt) suppliers may include 35589-28-7 (mono-hydrochloride salt) API manufacturers, exporters, distributors and traders.
click here to find a list of 35589-28-7 (mono-hydrochloride salt) suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
We have 80 companies offering 35589-28-7 (mono-hydrochloride salt)
Get in contact with the supplier of your choice: