Egis is a Hungarian generic pharma company with 110 years history. Our activities incorporate all areas of the pharma value chain.
01 1Egis Pharmaceuticals PLC
02 2Neuland Laboratories Limited
03 1APICORE PHARMACEUTICALS PRIVATE LIMITED
04 1Enaltec Labs Private Limited
05 2Olon S.p.A.
06 1Sionc Pharmaceutical Private Limited
07 1Zydus Lifesciences Limited
01 3ETHACRYNIC ACID
02 5Ethacrynic Acid
03 1Ethacrynic acid
01 1Hungary
02 6India
03 2Italy
Egis is a Hungarian generic pharma company with 110 years history. Our activities incorporate all areas of the pharma value chain.
NDC Package Code : 48581-320
Start Marketing Date : 2020-04-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
Neuland Laboratories- A dedicated 100% API provider.
NDC Package Code : 58032-1015
Start Marketing Date : 2013-11-20
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Neuland Laboratories- A dedicated 100% API provider.
NDC Package Code : 58032-2020
Start Marketing Date : 2017-12-19
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 42973-169
Start Marketing Date : 2012-05-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 42413-0059
Start Marketing Date : 2012-03-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17337-0401
Start Marketing Date : 2017-07-19
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17337-0429
Start Marketing Date : 2017-07-19
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 76055-0022
Start Marketing Date : 2019-12-31
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65841-175
Start Marketing Date : 2014-03-14
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Ethacrynic Acid manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ethacrynic Acid, including repackagers and relabelers. The FDA regulates Ethacrynic Acid manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ethacrynic Acid API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Ethacrynic Acid manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ethacrynic Acid supplier is an individual or a company that provides Ethacrynic Acid active pharmaceutical ingredient (API) or Ethacrynic Acid finished formulations upon request. The Ethacrynic Acid suppliers may include Ethacrynic Acid API manufacturers, exporters, distributors and traders.
click here to find a list of Ethacrynic Acid suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Ethacrynic Acid as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Ethacrynic Acid API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture Ethacrynic Acid as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain Ethacrynic Acid and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Ethacrynic Acid NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Ethacrynic Acid suppliers with NDC on PharmaCompass.
We have 7 companies offering Ethacrynic Acid
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