EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
01 1EUROAPI Germany GmbH
02 2Assia Chemical Industries Ltd - Teva Tech Site
03 1Curia India Private Limited
04 1DARMERICA, LLC
05 2F.I.S. FABBRICA ITALIANA SINTETICI S.P.A.
06 2Ipca Laboratories Limited
07 1KALCHEM INTERNATIONAL INC
08 1KALINTIS HEALTHCARE PRIVATE LIMITED
09 1LETCO MEDICAL, LLC
10 1Medisca
11 1Olon S.p.A.
12 1Professional Compounding Centers of America
13 1Professional Compounding Centers of America dba PCCA
14 1SMS Lifesciences India Limited
15 1Spectrum Laboratory Products, Inc.
16 1Sri Krishna Pharmaceuticals Ltd. Unit I
01 8FUROSEMIDE
02 10Furosemide
03 1Furosemide Micro
01 1France
02 5India
03 2Israel
04 3Italy
05 6U.S.A
06 2United Kingdom
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
NDC Package Code : 82348-105
Start Marketing Date : 1995-12-18
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 48087-0053
Start Marketing Date : 2010-03-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 48087-0054
Start Marketing Date : 2010-03-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 57451-0006
Start Marketing Date : 2012-02-28
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 57451-0007
Start Marketing Date : 2012-02-28
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-3306
Start Marketing Date : 2024-03-05
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17337-0087
Start Marketing Date : 2019-03-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-0078
Start Marketing Date : 2019-11-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 51927-0342
Start Marketing Date : 2024-07-02
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 49452-3222
Start Marketing Date : 1997-08-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
A Diumide-K manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Diumide-K, including repackagers and relabelers. The FDA regulates Diumide-K manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Diumide-K 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 Diumide-K manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Diumide-K supplier is an individual or a company that provides Diumide-K active pharmaceutical ingredient (API) or Diumide-K finished formulations upon request. The Diumide-K suppliers may include Diumide-K API manufacturers, exporters, distributors and traders.
click here to find a list of Diumide-K 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 Diumide-K as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Diumide-K 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 Diumide-K 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 Diumide-K and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Diumide-K NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Diumide-K suppliers with NDC on PharmaCompass.
We have 15 companies offering Diumide-K
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