Shandong Loncom is an R&D-focused manufacturer of Anti-cancer APIs.
01 1Shandong Loncom Pharmaceutical
02 1Ajinomoto Company
03 1Aurore Life Sciences
04 1Bulat Pharmaceutical
05 1Guangzhou Tosun Pharmaceutical
06 2Kanto Chemical
07 2Katsura Chemical
08 1Kukjeon Pharmaceutical
09 1Nippi
10 1Permachem Asia, Ltd
11 1Prajna Generics
12 1Tianjin Hankang Pharmaceutical Biotechnology
01 3China
02 3India
03 7Japan
04 1South Korea
01 2Active
02 12Blank
01 14Blank
01 1217MF11135
02 1218MF10299
03 1220MF10115
04 1220MF10201
05 1220MF10222
06 1223MF10091
07 1226MF10002
08 7Blank
01 14Blank
Shandong Loncom is an R&D-focused manufacturer of Anti-cancer APIs.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 36042
Submission : 2021-12-09
Status : Active
Type : II
Registration Number : 223MF10091
Registrant's Address : 4-15-19 Hibarigaoka, Zama City, Kanagawa Prefecture
Initial Date of Registration : 2011-06-29
Latest Date of Registration : --
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 36046
Submission : 2021-07-03
Status : Active
Type : II
NDC Package Code : 72761-028
Start Marketing Date : 2020-07-25
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registration Number : 220MF10222
Registrant's Address : 3-2-8 Nihonbashi Honcho, Chuo-ku, Tokyo
Initial Date of Registration : 2008-11-04
Latest Date of Registration : --
Registration Number : 217MF11135
Registrant's Address : 1-10-11, Nihonbashi Horidomecho, Chuo-ku, Tokyo
Initial Date of Registration : 2005-12-05
Latest Date of Registration : --
Registration Number : 220MF10201
Registrant's Address : 4-15-19 Hibarigaoka, Zama City, Kanagawa Prefecture
Initial Date of Registration : 2008-09-19
Latest Date of Registration : --
Registration Number : 220MF10115
Registrant's Address : 129 Suidocho, Aoi Ward, Shizuoka City, Shizuoka Prefecture
Initial Date of Registration : 2008-04-21
Latest Date of Registration : --
Registrant Name : Kukjeon Pharmaceutical Co., Ltd.
Registration Date : 2014-08-01
Registration Number : 2520-14-ND
Manufacturer Name : Kukjeon Pharmaceutical Co., Ltd.
Manufacturer Address : 8, Balan Industrial Complex-ro, Hyangnam-eup, Hwaseong-si, Gyeonggi-do
Registration Number : 226MF10002
Registrant's Address : 1-15-1 Kyobashi, Chuo-ku, Tokyo
Initial Date of Registration : 2014-01-08
Latest Date of Registration : --
Registration Number : 218MF10299
Registrant's Address : 3-2-8 Nihonbashi Honcho, Chuo-ku, Tokyo
Initial Date of Registration : 2006-02-28
Latest Date of Registration : --
A Nafamostat manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nafamostat, including repackagers and relabelers. The FDA regulates Nafamostat manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nafamostat 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 Nafamostat supplier is an individual or a company that provides Nafamostat active pharmaceutical ingredient (API) or Nafamostat finished formulations upon request. The Nafamostat suppliers may include Nafamostat API manufacturers, exporters, distributors and traders.
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