Suanfarma, at the Core of a Better Life.
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01 1Suanfarma
02 1Archimica
03 1Bristol Myers Squibb
04 1FUJIAN FUKANG PHARMACEUTICAL
05 2Fermic
06 1Gyma Laboratories of America
07 1Ningxia Kingvit Pharmaceutical Co Ltd
08 1Ningxia Qiyuan Pharmaceutical
09 8Pfizer Inc
10 1Roche Diagnostics GmbH
11 1Sichuan Sunnyhope Pharmaceutical
12 1XIAN LIJUN PHARMACEUTICAL
13 6Blank
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01 25TETRACYCLINE HYDROCHLORIDE
02 1TOPICYCLINE
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01 5China
02 1Germany
03 1Italy
04 2Mexico
05 1Spain
06 10U.S.A
07 6Blank
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01 5Active
02 21Inactive
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01 3Complete
02 23Blank
GDUFA
DMF Review : Complete
Rev. Date : 2014-01-24
Pay. Date : 2013-07-31
DMF Number : 13339
Submission : 1998-09-01
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13288
Submission : 1998-09-01
Status : Inactive
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2020-03-20
Pay. Date : 2020-03-18
DMF Number : 33499
Submission : 2019-01-14
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2014-05-16
Pay. Date : 2014-04-30
DMF Number : 22356
Submission : 2008-12-19
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13365
Submission : 1998-09-01
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 11919
Submission : 1996-04-09
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13718
Submission : 1998-09-01
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13659
Submission : 1998-09-01
Status : Active
Type : II
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13348
Submission : 1998-09-01
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13357
Submission : 1998-09-01
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
A Actisite manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Actisite, including repackagers and relabelers. The FDA regulates Actisite manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Actisite 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 Actisite manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Actisite supplier is an individual or a company that provides Actisite active pharmaceutical ingredient (API) or Actisite finished formulations upon request. The Actisite suppliers may include Actisite API manufacturers, exporters, distributors and traders.
click here to find a list of Actisite suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Actisite DMF (Drug Master File) is a document detailing the whole manufacturing process of Actisite active pharmaceutical ingredient (API) in detail. Different forms of Actisite DMFs exist exist since differing nations have different regulations, such as Actisite USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Actisite DMF submitted to regulatory agencies in the US is known as a USDMF. Actisite USDMF includes data on Actisite's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Actisite USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Actisite suppliers with USDMF on PharmaCompass.
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