LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
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01 1LGM Pharma
02 1Ahk Tech
03 1Apotex Pharmachem
04 2Archimica
05 1Asahi Kasei Finechem
06 1Axitec
07 1Biesterfeld Spezialchemie GmbH
08 1Fujian South Pharmaceutical
09 1Guangzhou Tosun Pharmaceutical
10 1Kekule Pharma
11 1Linnea SA
12 1Mac-Chem Products (India) Pvt.Ltd
13 1Pfizer Inc
14 1Roche Diagnostics GmbH
15 1Sakar Healthcare
16 1Shenzhen Haorui
17 1Shouyuan Chemical
18 1Surajlok Chemicals
19 1Tecoland Corporation
20 1Vannsh Life Sciences
21 1Yamasa Corporation
22 1Zhejiang Hisun Pharmaceutical
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02 7China
03 2Germany
04 5India
05 2Italy
06 2Japan
07 1Switzerland
08 3U.S.A
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01 3Active
02 12Inactive
03 13Blank
01 4Valid
02 1Withdrawn by Holder
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01 1217MF10811
02 1218MF10475
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01 1WC-0275
02 1WC-0435
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LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-01-18
Pay. Date : 2012-12-18
DMF Number : 15959
Submission : 2002-04-28
Status : Active
Type : II
Certificate Number : R1-CEP 2001-390 - Rev 03
Issue Date : 2016-08-02
Type : Chemical
Substance Number : 760
Status : Withdrawn by Holder
NDC Package Code : 58623-0026
Start Marketing Date : 2004-01-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2017-06-30
Pay. Date : 2017-06-08
DMF Number : 6215
Submission : 1986-01-23
Status : Active
Type : II
Certificate Number : CEP 2017-218 - Rev 03
Issue Date : 2024-09-20
Type : Chemical
Substance Number : 760
Status : Valid
Registration Number : 217MF10811
Registrant's Address : 3-3-23 Nakanoshima, Kita-ku, Osaka City, Osaka Prefecture
Initial Date of Registration : 2005-11-01
Latest Date of Registration :
NDC Package Code : 12848-1003
Start Marketing Date : 1986-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : DRUG FOR FURTHER PROCESSING
Registrant Name : Handok Co., Ltd.
Registration Date : 2022-07-13
Registration Number : 20220713-210-J-1332
Manufacturer Name : Asahi Kasei Finechem Co., Ltd. Nobeoka Pharmaceuticals Plant
Manufacturer Address : 6-2633-7 Asahimachi, Nobeoka, Miyazaki 882-0847, Japan
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-12-18
Pay. Date : 2013-01-15
DMF Number : 25267
Submission : 2011-09-07
Status : Active
Type : II
Certificate Number : R1-CEP 2000-048 - Rev 04
Issue Date : 2020-10-16
Type : Chemical
Substance Number : 760
Status : Valid
NDC Package Code : 55512-0026
Start Marketing Date : 2019-12-17
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 26281
Submission : 2012-05-24
Status : Inactive
Type : II
Certificate Number : CEP 2012-251 - Rev 02
Issue Date : 2024-04-30
Type : Chemical
Substance Number : 760
Status : Valid
Date of Issue : 2021-01-22
Valid Till : 2023-08-01
Written Confirmation Number : WC-0275
Address of the Firm :
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 18071
Submission : 2005-01-21
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 1534
Submission : 1970-06-01
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 9468
Submission : 1991-12-18
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 7770
Submission : 1988-11-21
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 23469
Submission : 2010-01-12
Status : Inactive
Type : II
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PharmaCompass offers a list of Cytarabine 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 Cytarabine manufacturer or Cytarabine supplier for your needs.
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A Arabinoside, Cytosine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Arabinoside, Cytosine, including repackagers and relabelers. The FDA regulates Arabinoside, Cytosine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Arabinoside, Cytosine 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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We have 22 companies offering Arabinoside, Cytosine
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