01 1Abbott Laboratories
02 1Cilag AG
03 1Corden Pharma Bergamo S.p.A
04 1Siegfried AG
05 1Solara Active Pharma Sciences
06 1Viatris
01 3DISULFIRAM
02 1DISULFIRAM MANUF & SOLD UNDER SIEGFRIED LABEL
03 2DISULFIRAM USP
01 1India
02 1Italy
03 2Switzerland
04 2U.S.A
01 3Active
02 3Inactive
01 2Complete
02 4Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 6117
Submission : 1985-12-10
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 5754
Submission : 1985-03-20
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 15041
Submission : 2000-09-15
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 4986
Submission : 1983-06-17
Status : Inactive
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2024-03-12
Pay. Date : 2024-02-26
DMF Number : 33722
Submission : 2019-03-31
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2015-12-04
Pay. Date : 2015-09-18
DMF Number : 23288
Submission : 2009-11-20
Status : Active
Type : II
29
PharmaCompass offers a list of Sulfiram 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 Sulfiram manufacturer or Sulfiram supplier for your needs.
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PharmaCompass also assists you with knowing the Sulfiram API Price utilized in the formulation of products. Sulfiram API Price is not always fixed or binding as the Sulfiram Price is obtained through a variety of data sources. The Sulfiram Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Antabuse, Antabus, Disulfiram manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Antabuse, Antabus, Disulfiram, including repackagers and relabelers. The FDA regulates Antabuse, Antabus, Disulfiram manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Antabuse, Antabus, Disulfiram 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 Antabuse, Antabus, Disulfiram supplier is an individual or a company that provides Antabuse, Antabus, Disulfiram active pharmaceutical ingredient (API) or Antabuse, Antabus, Disulfiram finished formulations upon request. The Antabuse, Antabus, Disulfiram suppliers may include Antabuse, Antabus, Disulfiram API manufacturers, exporters, distributors and traders.
click here to find a list of Antabuse, Antabus, Disulfiram suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Antabuse, Antabus, Disulfiram DMF (Drug Master File) is a document detailing the whole manufacturing process of Antabuse, Antabus, Disulfiram active pharmaceutical ingredient (API) in detail. Different forms of Antabuse, Antabus, Disulfiram DMFs exist exist since differing nations have different regulations, such as Antabuse, Antabus, Disulfiram USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Antabuse, Antabus, Disulfiram DMF submitted to regulatory agencies in the US is known as a USDMF. Antabuse, Antabus, Disulfiram USDMF includes data on Antabuse, Antabus, Disulfiram's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Antabuse, Antabus, Disulfiram USDMF is kept confidential to protect the manufacturer’s intellectual property.
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