Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
01 1NURAY CHEMICALS PRIVATE LIMITED
02 1Azico Biophore India Private Limited
03 1DARMERICA, LLC
04 1Fagron Inc
05 1Guang’an Kingday Pharma & Chem Co., Ltd.
06 1LETCO MEDICAL, LLC
07 1Lundbeck Pharmaceuticals Italy S.p.A.
08 1MAEDA INC
09 1MEDISCA INC.
10 1MSN Laboratories Private Limited
11 1Medisca Inc.
12 1Professional Compounding Centers of America
13 1Professional Compounding Centers of America dba PCCA
14 1STHREE CHEMICALS PRIVATE LIMITED
01 3DIAZOXIDE
02 11Diazoxide
01 1China
02 1Denmark
03 3India
04 1Netherlands
05 4U.S.A
06 2United Kingdom
07 2Blank
Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
NDC Package Code : 58159-039
Start Marketing Date : 2023-11-08
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (35kg/35kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51552-1582
Start Marketing Date : 2020-12-21
End Marketing Date : 2026-09-30
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 52952-003
Start Marketing Date : 2012-07-25
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 45562-1740
Start Marketing Date : 2022-01-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : DRUG FOR FURTHER PROCESSING
NDC Package Code : 62991-2857
Start Marketing Date : 2010-10-06
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 38779-0324
Start Marketing Date : 2014-07-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-3184
Start Marketing Date : 2020-02-04
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 14501-0096
Start Marketing Date : 2020-02-19
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-0297
Start Marketing Date : 2023-03-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (35kg/35kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 51927-2742
Start Marketing Date : 2013-06-25
End Marketing Date : 2025-05-27
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
A Diazoxide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Diazoxide, including repackagers and relabelers. The FDA regulates Diazoxide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Diazoxide 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 Diazoxide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Diazoxide supplier is an individual or a company that provides Diazoxide active pharmaceutical ingredient (API) or Diazoxide finished formulations upon request. The Diazoxide suppliers may include Diazoxide API manufacturers, exporters, distributors and traders.
click here to find a list of Diazoxide 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 Diazoxide as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Diazoxide 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 Diazoxide 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 Diazoxide and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Diazoxide NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Diazoxide suppliers with NDC on PharmaCompass.
We have 10 companies offering Diazoxide
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