European CDMO and Gx manufacturer with 75 years of experience in delivering premium APIs to pharmaceutical partners worldwide.

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01 1Polpharma
02 1Jai Radhe Sales
03 1ASolution Pharmaceuticals
04 1Tenatra Exports
05 1AXYNTIS Group
06 1Abbott Laboratories
07 1Apicore
08 1Chongqing Huapont Pharmaceutical
09 1Cilag AG
10 1Corden Pharma Bergamo S.p.A
11 1Piramal Pharma Solutions
12 1Qfine Synthesis
13 1SNA Healthcare
14 1Siegfried AG
15 1Solara Active Pharma Sciences
16 1Speichim Processing
17 1Tianish Laboratories
18 1Viatris
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01 1China
02 2France
03 7India
04 1Italy
05 1Poland
06 1Spain
07 2Switzerland
08 3U.S.A
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01 3Active
02 3Inactive
03 12Blank
01 1Valid
02 17Blank
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01 18Blank
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01 1WC-0110n
02 1WC-0294
03 16Blank
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01 18Blank
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01 142973-137
02 148943-0015
03 149964-0032
04 172643-028
05 184206-0115
06 13Blank
01 18Blank
European CDMO and Gx manufacturer with 75 years of experience in delivering premium APIs to pharmaceutical partners worldwide.
Tenatra connects Indian manufacturers with global buyers through active partners in Germany, Switzerland, Belgium, Spain & Turkey.
GDUFA
DMF Review : Reviewed
Rev. Date : 2015-12-04
Pay. Date : 2015-09-18
DMF Number : 23288
Submission : 2009-11-20
Status : Active
Type : II

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 15041
Submission : 2000-09-15
Status : Active
Type : II
NDC Package Code : 49964-0032
Start Marketing Date : 2009-09-24
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT

GDUFA
DMF Review : Reviewed
Rev. Date : 2024-03-12
Pay. Date : 2024-02-26
DMF Number : 33722
Submission : 2019-03-31
Status : Active
Type : II
Certificate Number : CEP 2019-197 - Rev 02
Issue Date : 2025-05-23
Type : Chemical
Substance Number : 603
Status : Valid
Date of Issue : 2024-05-29
Valid Till : 2027-03-04
Written Confirmation Number : WC-0294
Address of the Firm :
NDC Package Code : 72643-028
Start Marketing Date : 2022-03-07
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 4986
Submission : 1983-06-17
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 : 6117
Submission : 1985-12-10
Status : Inactive
Type : II

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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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A Disulfiram manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Disulfiram, including repackagers and relabelers. The FDA regulates Disulfiram manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 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 Disulfiram supplier is an individual or a company that provides Disulfiram active pharmaceutical ingredient (API) or Disulfiram finished formulations upon request. The Disulfiram suppliers may include Disulfiram API manufacturers, exporters, distributors and traders.
click here to find a list of Disulfiram suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
We have 18 companies offering Disulfiram
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