Malladi is a leader in Ephedrine, Pseudoephedrine Salts & Phenylephrine HCl // USFDA, EDQM, ANSM, KFDA, and TGA inspected.

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01 1Malladi Drugs & Pharmaceuticals Limited
02 1TAPI Technology & API Services
03 1API Corporation
04 1Actavis Inc
05 1Arch Pharmalabs
06 1Chemi SpA
07 10Divis Laboratories
08 2Erregierre SpA
09 1Esteve Quimica
10 1GSK
11 1Hengdian Group
12 1Hetero Drugs
13 4Ipca Laboratories
14 1Jiangsu Zhongdan Chemical
15 1Lupin Ltd
16 1Napp Technologies
17 2Recordati
18 1Southwest Synthetic Pharmaceutical
19 1Viatris
20 1Zhejiang Shenzhou Pharmaceutical
21 2Blank
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01 4China
02 18India
03 1Ireland
04 1Israel
05 5Italy
06 1Japan
07 1Spain
08 2U.S.A
09 1United Kingdom
10 2Blank
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01 6Active
02 14Inactive
03 16Blank
01 3Valid
02 2Withdrawn by Holder
03 31Blank
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01 1224MF10109
02 1228MF10204
03 34Blank
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01 1WC-0031
02 1WC-0066
03 1WC-0254
04 33Blank
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01 120050831-2-C-57-01
02 120050831-2-C-58-02
03 120050831-2-C-58-02(10)
04 120050831-2-C-58-02(11)
05 120050831-2-C-58-02(12)
06 120050831-2-C-58-02(3)
07 120050831-2-C-58-02(4)
08 120050831-2-C-58-02(5)
09 120050831-2-C-58-02(6)
10 120050831-2-C-58-02(8)
11 120050831-2-C-58-02(9)
12 120050831-2-C-59-03
13 120050831-2-C-63-06
14 120050831-2-C-63-06(6)
15 120050831-2-C-63-06(7)
16 120050831-2-C-63-06(8)
17 20Blank
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01 149706-0681
02 262331-008
03 165977-0082
04 32Blank
01 36Blank
Malladi is a leader in Ephedrine, Pseudoephedrine Salts & Phenylephrine HCl // USFDA, EDQM, ANSM, KFDA, and TGA inspected.
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
Certificate Number : CEP 2000-115 - Rev 13
Issue Date : 2025-03-12
Type : Chemical
Substance Number : 1350
Status : Valid
GDUFA
DMF Review : Reviewed
Rev. Date : 2014-07-08
Pay. Date : 2013-05-03
DMF Number : 18581
Submission : 2005-06-24
Status : Active
Type : II

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 14174
Submission : 1999-06-04
Status : Inactive
Type : II

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 18976
Submission : 2007-04-08
Status : Inactive
Type : II

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13105
Submission : 1998-07-30
Status : Inactive
Type : II

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 15491
Submission : 2001-06-15
Status : Inactive
Type : II

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 11984
Submission : 1996-06-03
Status : Inactive
Type : II

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 12445
Submission : 1997-03-18
Status : Inactive
Type : II

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 14804
Submission : 2000-03-23
Status : Inactive
Type : II
Registrant Name : Chodang Pharmaceutical Co., Ltd.
Registration Date : 2005-08-31
Registration Number : 20050831-2-C-57-01
Manufacturer Name : ZHEJIANG SHENZHOU Pharmaceutical Co., Ltd
Manufacturer Address : No.14 Chuancheng Nan road 317300 Xianju, Zhejiang

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PharmaCompass offers a list of Nabumetone API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Nabumetone manufacturer or Nabumetone supplier for your needs.
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A Listran manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Listran, including repackagers and relabelers. The FDA regulates Listran manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Listran 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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