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 114593-871
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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.
GDUFA
DMF Review : Reviewed
Rev. Date : 2021-06-10
Pay. Date : 2021-06-07
DMF Number : 7882
Submission : 1989-01-24
Status : Active
Type : II
Certificate Number : R1-CEP 2008-279 - Rev 02
Issue Date : 2023-01-12
Type : Chemical
Substance Number : 524
Status : Valid
Registration Number : 307MF10033
Registrant's Address : H-1106 BUDAPEST KERESZTURI UT 30-38 HUNGARY
Initial Date of Registration : 2025-02-07
Latest Date of Registration :
NDC Package Code : 48581-114
Start Marketing Date : 2007-05-04
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Available Reg Filing : BR |
NDC Package Code : 82298-902
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 : 2013-02-26
Pay. Date : 2013-02-13
DMF Number : 1949
Submission : 1972-06-09
Status : Active
Type : II
Certificate Number : CEP 1992-002 - Rev 07
Issue Date : 2024-02-15
Type : Chemical
Substance Number : 524
Status : Valid
NDC Package Code : 50396-7517
Start Marketing Date : 2011-06-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Tenatra connects Indian manufacturers with global buyers through active partners in Germany, Switzerland, Belgium, Spain & Turkey.
Date of Issue : 2022-07-27
Valid Till : 2025-07-29
Written Confirmation Number : WC-0179
Address of the Firm :
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 11888
Submission : 1996-03-08
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 1955
Submission : 1972-06-19
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3039
Submission : 1977-10-10
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
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DMF Number : 18173
Submission : 2005-03-02
Status : Inactive
Type : II
32
PharmaCompass offers a list of Promethazine Hydrochloride 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 Promethazine Hydrochloride manufacturer or Promethazine Hydrochloride supplier for your needs.
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A Promethazine.HCl manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Promethazine.HCl, including repackagers and relabelers. The FDA regulates Promethazine.HCl manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Promethazine.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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A Promethazine.HCl supplier is an individual or a company that provides Promethazine.HCl active pharmaceutical ingredient (API) or Promethazine.HCl finished formulations upon request. The Promethazine.HCl suppliers may include Promethazine.HCl API manufacturers, exporters, distributors and traders.
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We have 25 companies offering Promethazine.HCl
Get in contact with the supplier of your choice: