Transo-Pharm GmbH works globally to supply Active Pharmaceutical Ingredients adhering to the highest quality & GMP standards.
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01 1Transo-Pharm Handels GmbH
02 1LGM Pharma
03 1Transo-Pharm USA LLC
04 1DKSH
05 1Jai Radhe Sales
06 1TAPI Technology & API Services
07 1ChemExpress
08 1Adorkem Technology S.p.A.
09 1Aspen Bio
10 2Boryung Pharmaceutical Co., Ltd
11 1Cerata Pharmaceuticals
12 1Concord Biotech
13 1DZD Heze Pharmaceutical Co Ltd
14 1Gemini PharmChem
15 1Gemini Pharmaceutical
16 1Guangzhou Topwork Chemical
17 1Hangzhou Longshine Bio-Tech
18 4Intas Pharmaceuticals
19 1Jiwan Pharmaceutical Technology Co., Ltd
20 2Meiji Seika Pharma
21 1MicroBiopharm Japan
22 3Olon S.p.A
23 2Pfizer Inc
24 1RPG Life Sciences
25 1Sakar Healthcare
26 1Sicor
27 1Sicor Societa Italiana Corticosteroidi Srl
28 1Sicor Spa
29 1Sterling Biotech
30 1Sun-shine Chem
31 1Synbias Pharma
32 1Synbias Pharma Limited Liability Company
33 1Tecoland Corporation
34 1Teva Pharmaceutical Industries
35 1Zhejiang Hisun Chemical Co., Ltd.
36 2Zhejiang Hisun Pharmaceutical
37 1Zhejiang Huida Biotech
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05 7Italy
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07 2South Korea
08 2Switzerland
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01 11Active
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01 1Expired
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01 1218MF10960
02 1223MF10126
03 1226MF10124
04 1302MF10073
05 1303MF10121
06 1305MF10028
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01 1WC-0292
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01 120201116-210-J-443
02 120201116-210-J-443(1)
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04 120201116-210-J-443(3)
05 120210217-210-J-674
06 120210315-210-J-875
07 120210420-210-J-515
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09 120210420-210-J-515(A)
10 120220124-210-J-1118
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01 112543-3209
02 117337-0260
03 153183-7000
04 156161-101
05 158623-0029
06 158623-0119
07 177391-001
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Transo-Pharm GmbH works globally to supply Active Pharmaceutical Ingredients adhering to the highest quality & GMP standards.
Certificate Number : R1-CEP 2004-059 - Rev 03
Issue Date : 2023-03-06
Type : Chemical
Substance Number : 714
Status : Valid
LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
GDUFA
DMF Review : Reviewed
Rev. Date : 2012-11-29
Pay. Date : 2012-11-08
DMF Number : 13726
Submission : 1998-09-01
Status : Active
Type : II
Certificate Number : CEP 2003-111 - Rev 07
Issue Date : 2025-07-28
Type : Chemical
Substance Number : 714
Status : Valid
Available Reg Filing : CA, ASMF |
ChemExpress delivers end-to-end CRO & CDMO solutions for small molecules, biologics & new modalities with ICH-grade quality.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 24858
Submission : 2011-04-05
Status : Active
Type : II
Certificate Number : R1-CEP 2012-039 - Rev 01
Issue Date : 2020-01-02
Type : Chemical
Substance Number : 714
Status : Valid
Date of Issue : 2024-02-28
Valid Till : 2026-12-16
Written Confirmation Number : WC-0292
Address of the Firm :
GDUFA
DMF Review : Reviewed
Rev. Date : 2017-10-18
Pay. Date : 2015-12-28
DMF Number : 13209
Submission : 1998-04-30
Status : Active
Type : II
Certificate Number : R1-CEP 2003-151 - Rev 03
Issue Date : 2020-04-02
Type : Chemical
Substance Number : 714
Status : Valid
Registration Number : 302MF10073
Registrant's Address : 2-4-16 Kyobashi, Chuo-ku, Tokyo
Initial Date of Registration : 2020-07-01
Latest Date of Registration :
NDC Package Code : 12543-3209
Start Marketing Date : 2010-01-14
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (10g/10g)
Marketing Category : BULK INGREDIENT
Registrant Name : BANTIVE KOREA CORP.
Registration Date : 2021-02-17
Registration Number : 20210217-210-J-674
Manufacturer Name : Meiji Seika Pharma Co., Ltd. Kitakami Plant
Manufacturer Address : 3-3, Kitakogyodanchi Kitakami-shi, Iwate-ken 024-0193, Japan
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 24128
Submission : 2010-08-31
Status : Inactive
Type : II
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PharmaCompass offers a list of Doxorubicin Hydrochloride 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 Doxorubicin Hydrochloride manufacturer or Doxorubicin Hydrochloride supplier for your needs.
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A Adriblastine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Adriblastine, including repackagers and relabelers. The FDA regulates Adriblastine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Adriblastine 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 Adriblastine supplier is an individual or a company that provides Adriblastine active pharmaceutical ingredient (API) or Adriblastine finished formulations upon request. The Adriblastine suppliers may include Adriblastine API manufacturers, exporters, distributors and traders.
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We have 37 companies offering Adriblastine
Get in contact with the supplier of your choice: