Siegfried – A global CDMO delivering integrated pharmaceutical development and manufacturing solutions.

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01 1Siegfried AG
02 1Corden Pharma Bergamo S.p.A
03 1Seratec SAS
04 1Wockhardt
05 3Blank
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01 5BETHANECHOL CHLORIDE
02 2BETHANECHOL CHLORIDE USP
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01 1France
02 1India
03 1Italy
04 1Switzerland
05 3Blank
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01 3Active
02 4Inactive
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01 1Complete
02 6Blank
Siegfried – A global CDMO delivering integrated pharmaceutical development and manufacturing solutions.
GDUFA
DMF Review : Complete
Rev. Date : 2018-12-28
Pay. Date : 2018-12-20
DMF Number : 15737
Submission : 2001-11-21
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 15213
Submission : 2000-12-20
Status : Inactive
Type : II

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 15866
Submission : 2002-02-18
Status : Active
Type : II

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 16119
Submission : 2002-08-27
Status : Active
Type : II

USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 4766
Submission : 1982-12-10
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 : 4348
Submission : 1981-12-08
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 : 2501
Submission : 1975-07-25
Status : Inactive
Type : II

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