Zhejiang Hengkang Pharm Group is a dynamic pharmaceutical entity, spanning drug research, large-scale production, and global marketing.

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01 1Zhejiang Hengkang Pharmaceutical
02 1Neuland Laboratories
03 1TAPI Technology & API Services
04 1Actavis Inc
05 1Akums Lifesciences
06 1Alembic Pharmaceuticals Limited
07 1Alivus Life Sciences
08 1Amoli Organics
09 1Apotex Pharmachem
10 1Aurobindo Pharma Limited
11 1Biocon
12 2CTX Lifesciences
13 1Cipla
14 1Erregierre SpA
15 1Jubilant Generics
16 1MSN Laboratories
17 1Medilux Laboratories
18 1Piramal Pharma Solutions
19 1SMS Pharmaceuticals
20 1Sun Pharmaceutical Industries Limited
21 1Symed Labs
22 1Viatris
23 2Waterstone Pharmaceuticals Inc.
24 1YUNG ZIP CHEMICAL INDUSTRIAL
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01 25DEFERASIROX
02 1DEFERASIROX [ROUTE CODE - "DR"]
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01 1Canada
02 3China
03 16India
04 1Ireland
05 1Israel
06 1Italy
07 1Taiwan
08 2U.S.A
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01 22Active
02 4Inactive
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01 14Complete
02 12Blank
Zhejiang Hengkang Pharm Group is a dynamic pharmaceutical entity, spanning drug research, large-scale production, and global marketing.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 41051
Submission : 2024-12-31
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2016-04-15
Pay. Date : 2016-03-17
DMF Number : 25733
Submission : 2012-01-26
Status : Active
Type : II
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
GDUFA
DMF Review : Complete
Rev. Date : 2014-02-20
Pay. Date : 2013-10-24
DMF Number : 27648
Submission : 2014-01-08
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 25964
Submission : 2012-03-27
Status : Active
Type : II

GDUFA
DMF Review : Complete
Rev. Date : 2017-01-05
Pay. Date : 2016-07-19
DMF Number : 26833
Submission : 2013-02-27
Status : Active
Type : II

GDUFA
DMF Review : Complete
Rev. Date : 2016-03-03
Pay. Date : 2016-02-18
DMF Number : 24209
Submission : 2010-10-28
Status : Active
Type : II

GDUFA
DMF Review : Complete
Rev. Date : 2015-04-06
Pay. Date : 2014-12-08
DMF Number : 28626
Submission : 2015-01-02
Status : Active
Type : II

GDUFA
DMF Review : Complete
Rev. Date : 2017-06-16
Pay. Date : 2017-05-25
DMF Number : 25888
Submission : 2012-03-30
Status : Active
Type : II

GDUFA
DMF Review : Complete
Rev. Date : 2015-06-09
Pay. Date : 2015-04-07
DMF Number : 25837
Submission : 2012-02-21
Status : Active
Type : II

GDUFA
DMF Review : Complete
Rev. Date : 2013-09-10
Pay. Date : 2013-09-03
DMF Number : 22369
Submission : 2008-12-20
Status : Active
Type : II

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A Deferasirox manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Deferasirox, including repackagers and relabelers. The FDA regulates Deferasirox manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Deferasirox 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 Deferasirox supplier is an individual or a company that provides Deferasirox active pharmaceutical ingredient (API) or Deferasirox finished formulations upon request. The Deferasirox suppliers may include Deferasirox API manufacturers, exporters, distributors and traders.
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A Deferasirox DMF (Drug Master File) is a document detailing the whole manufacturing process of Deferasirox active pharmaceutical ingredient (API) in detail. Different forms of Deferasirox DMFs exist exist since differing nations have different regulations, such as Deferasirox USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Deferasirox DMF submitted to regulatory agencies in the US is known as a USDMF. Deferasirox USDMF includes data on Deferasirox's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Deferasirox USDMF is kept confidential to protect the manufacturer’s intellectual property.
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