Maithri Drugs: Dedicated to your API needs.

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01 1Maithri Drugs
02 1Aurore Life Sciences
03 1Centaur Pharmaceuticals
04 2Cheer Fine Pharmaceutical
05 1Chieron Active Ingredients
06 1Daiwa Pharmaceuticals
07 1Delta Finochem
08 1DongWha Pharm
09 1DongWoo Syntech
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17 3Jiangsu Zenji Pharmaceuticals,Ltd.
18 46Jiangxi Synergy Pharmaceutical
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23 1Macleods Pharmaceuticals Limited
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26 1Otsuka Chemical Co Ltd
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29 1Sam-Oh Pharm Co. Ltd
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36 2Suzhou Tianma Pharma Group Co Ltd
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01 1Active
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01 1218MF10724
02 1218MF10732
03 1218MF10849
04 1218MF10919
05 1220MF10002
06 1221MF10056
07 1222MF10036
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09 1222MF10140
10 1222MF10239
11 1222MF10259
12 1223MF10143
13 1224MF10078
14 1227MF10124
15 1228MF10089
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18 1230MF10081
19 1305MF10002
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01 1WC-0079
02 1WC-0542
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01 120050831-4-B-12-02
02 120050831-4-B-15-04
03 120050831-4-B-16-05
04 120050831-4-B-17-06
05 120050831-4-B-21-09
06 120050905-4-B-22-10
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56 120081031-4-B-287-15
57 120110805-4-B-320-16
58 120120302-4-B-329-18
59 120120927-4-B-353-19
60 120160725-4-B-387-21
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69 120210107-4-B-439-22
70 120241002-4-B-480-23
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01 152048-1982
02 171666-021
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GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 43855
Submission : 2026-03-30
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 21700
Submission : 2008-06-09
Status : Inactive
Type : II
Registration Number : 228MF10089
Registrant's Address : Jiangxi Fengxin Industrial Park, Fengxin, 330700, Jiangxi Province, P. R. China
Initial Date of Registration : 2016-04-15
Latest Date of Registration :
NDC Package Code : 52048-1982
Start Marketing Date : 2009-07-17
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : International Pharmaceutical Co., Ltd.
Registration Date : 2026-02-12
Registration Number : 20070504-4-B-240-14(51)
Manufacturer Name : Jiangxi Synergy Pharmaceutical Co., Ltd
Manufacturer Address : No. 699, Changle Avenue, Jiangxi Fengxin Industrial Park, Fengxin County, 330700, Yichun City, Jiangxi Province, China

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 15001
Submission : 2000-08-10
Status : Inactive
Type : II



Registration Number : 222MF10259
Registrant's Address : 25, Barangongdan-ro, Hyangnam-eup, Hwaseong-si, Gyeonggi-do Korea
Initial Date of Registration : 2010-11-18
Latest Date of Registration :
Registrant Name : Polaris AI Pharma Co., Ltd.
Registration Date : 2012-09-27
Registration Number : 20120927-4-B-353-19
Manufacturer Name : Polaris AI Pharma Co., Ltd. @ [Manufacturer of Method II Product] Zenji Pharmaceuticals (Suzhou) Ltd.
Manufacturer Address : No. 10, No. 11, Block 34, Balan Industrial Complex, 25, Balan Gongdan-ro, Hyangnam-eup, Hwaseong-si, Gyeonggi-do @No.122. Xuqing Road, Xuguan Town, Suzhou, Jiangsu, China

Registration Number : 222MF10140
Registrant's Address : 25, Barangongdan-ro, Hyangnam-eup, Hwaseong-si, Gyeonggi-do, Korea
Initial Date of Registration : 2010-04-14
Latest Date of Registration :


Date of Issue : 2026-05-13
Valid Till : 2028-12-08
Written Confirmation Number : WC-0542
Address of the Firm :
Registrant Name : Iksoo Pharmaceutical Co., Ltd.
Registration Date : 2025-03-11
Registration Number : 20250311-4-B-485-24
Manufacturer Name : AURORE LIFE SCIENCES PRIVATE LIMITED
Manufacturer Address : Plot No. 180/2 & 3, Khazipally Village, Jinnaram Mandal, Sangareddy District, Pin Code 502319, Telangana State, India

Registration Number : 218MF10919
Registrant's Address : 5, Soonwha-dong, Joong-Ku, Seoul. Korea
Initial Date of Registration : 2006-11-21
Latest Date of Registration :
Registrant Name : Donghwa Pharmaceutical Co., Ltd.
Registration Date : 2005-08-31
Registration Number : 20050831-4-B-21-09
Manufacturer Name : Donghwa Pharmaceutical Co., Ltd.
Manufacturer Address : 167, Chungjusandan 1-ro, Chungju-si, Chungcheongbuk-do

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PharmaCompass offers a list of Rebamipide 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 Rebamipide manufacturer or Rebamipide supplier for your needs.
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A Rebagen manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Rebagen, including repackagers and relabelers. The FDA regulates Rebagen manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Rebagen 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 Rebagen supplier is an individual or a company that provides Rebagen active pharmaceutical ingredient (API) or Rebagen finished formulations upon request. The Rebagen suppliers may include Rebagen API manufacturers, exporters, distributors and traders.
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