TAPI offers customized CDMO Solutions for API development and manufacturing services.
01 1TAPI Technology & API Services
02 1DZD Heze Pharmaceutical Co Ltd
03 1Intas Pharmaceuticals
04 1Meiji Seika Pharma
05 1MicroBiopharm Japan
06 1Olon S.p.A
07 2Pfizer Inc
08 1RPG Life Sciences
09 1Sicor Spa
10 1Sterling Biotech
11 1Synbias Pharma Limited Liability Company
12 2Zhejiang Hisun Pharmaceutical
01 1DOXORUBICIN HCL
02 6DOXORUBICIN HYDROCHLORIDE
03 1DOXORUBICIN HYDROCHLORIDE DRUG SUBSTANCE
04 2DOXORUBICIN HYDROCHLORIDE USP
05 1DOXORUBICIN HYDROCHLORIDE USP (FERMENTATION)
06 1DOXORUBICIN HYDROCHLORIDE USP/EP
07 1DOXORUBICIN HYDROCHLORIDE(API)
08 1DOXORUBICIN HYDROCHLORIDE, LYOPHILIZED
01 3China
02 3India
03 1Israel
04 2Italy
05 2Japan
06 2U.S.A
07 1Ukraine
01 11Active
02 3Inactive
01 9Complete
02 5Blank
GDUFA
DMF Review : Complete
Rev. Date : 2012-11-29
Pay. Date : 2012-11-08
DMF Number : 13726
Submission : 1998-09-01
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2024-08-27
Pay. Date : 2024-07-18
DMF Number : 31153
Submission : 2016-11-11
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2017-10-18
Pay. Date : 2015-12-28
DMF Number : 13209
Submission : 1998-04-30
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2013-03-25
Pay. Date : 2012-11-13
DMF Number : 13211
Submission : 1998-04-30
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2019-04-22
Pay. Date : 2018-12-17
DMF Number : 30035
Submission : 2015-11-16
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 2098
Submission : 1973-04-27
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 24858
Submission : 2011-04-05
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2014-02-14
Pay. Date : 2014-01-28
DMF Number : 16178
Submission : 2002-10-09
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2013-11-12
Pay. Date : 2013-07-24
DMF Number : 27311
Submission : 2013-09-09
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2013-03-07
Pay. Date : 2012-12-18
DMF Number : 13773
Submission : 1998-09-01
Status : Active
Type : II
A Doxorubicin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Doxorubicin, including repackagers and relabelers. The FDA regulates Doxorubicin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Doxorubicin API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Doxorubicin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Doxorubicin supplier is an individual or a company that provides Doxorubicin active pharmaceutical ingredient (API) or Doxorubicin finished formulations upon request. The Doxorubicin suppliers may include Doxorubicin API manufacturers, exporters, distributors and traders.
click here to find a list of Doxorubicin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Doxorubicin DMF (Drug Master File) is a document detailing the whole manufacturing process of Doxorubicin active pharmaceutical ingredient (API) in detail. Different forms of Doxorubicin DMFs exist exist since differing nations have different regulations, such as Doxorubicin USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Doxorubicin DMF submitted to regulatory agencies in the US is known as a USDMF. Doxorubicin USDMF includes data on Doxorubicin's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Doxorubicin USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Doxorubicin suppliers with USDMF on PharmaCompass.
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