Egis is a Hungarian generic pharma company with 110 years history. Our activities incorporate all areas of the pharma value chain.
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01 1Egis Pharmaceuticals PLC
02 1EUROAPI
03 1Minakem (formerly Delmar Chemicals)
04 1Sanofi
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01 9Active
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01 1219MF10261
02 1222MF10096
03 1304MF10157
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01 1WC-0139
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01 138779-0423
02 142413-0137
03 150396-7515
04 162991-1425
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06 171554-002
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08 172166-004
09 173435-001
10 182298-901
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Egis is a Hungarian generic pharma company with 110 years history. Our activities incorporate all areas of the pharma value chain.
Certificate Number : R1-CEP 1996-077 - Rev 07
Issue Date : 2021-10-15
Type : Chemical
Substance Number : 475
Status : Valid
Registration Number : 304MF10157
Registrant's Address : H-1106 BUDAPEST KERESZTURI UT 30-38 HUNGARY
Initial Date of Registration : 2022-12-15
Latest Date of Registration :
Available Reg Filing : ASMF, BR |
Registration Number : 222MF10096
Registrant's Address : 82 Avenue Raspail 94250 Gentilly France
Initial Date of Registration : 2010-03-17
Latest Date of Registration :
NDC Package Code : 82298-901
Start Marketing Date : 2011-06-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-06-03
Pay. Date : 2013-02-13
DMF Number : 1516
Submission : 1970-04-23
Status : Active
Type : II
Certificate Number : CEP 1999-043 - Rev 08
Issue Date : 2024-02-16
Type : Chemical
Substance Number : 475
Status : Valid
NDC Package Code : 50396-7515
Start Marketing Date : 2011-06-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
GDUFA
DMF Review : Reviewed
Rev. Date : 2017-07-05
Pay. Date : 2017-06-19
DMF Number : 31479
Submission : 2017-06-17
Status : Active
Type : II
Certificate Number : R0-CEP 2021-266 - Rev 00
Issue Date : 2023-03-08
Type : Chemical
Substance Number : 475
Status : Valid
Date of Issue : 2021-10-22
Valid Till : 2024-10-21
Written Confirmation Number : WC-0511
Address of the Firm :
NDC Package Code : 73435-001
Start Marketing Date : 2019-11-05
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
Tenatra connects Indian manufacturers with global buyers through active partners in Germany, Switzerland, Belgium, Spain & Turkey.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 1616
Submission : 1970-07-02
Status : Inactive
Type : II
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A Chlorpromazine HCl manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Chlorpromazine HCl, including repackagers and relabelers. The FDA regulates Chlorpromazine HCl manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Chlorpromazine HCl 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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We have 37 companies offering Chlorpromazine HCl
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