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 1Apicore Pharmaceuticals Private Limited
03 1Clarochem Ireland Ltd
04 1Dasami Lab Private Limited
05 1MSN Life Sciences Private Limited
06 1Piramal Pharma Limited
07 1Quimica Sintetica S.A.
08 1Sumitomo Pharma Co., Ltd.
01 2DROXIDOPA
02 5Droxidopa
03 1Droxipoda
01 4India
02 1Ireland
03 1Japan
04 1Spain
05 1U.S.A
Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
NDC Package Code : 58159-049
Start Marketing Date : 2016-07-20
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (35kg/35kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 42973-237
Start Marketing Date : 2017-12-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 76278-1120
Start Marketing Date : 2016-11-25
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 70966-0006
Start Marketing Date : 2018-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 69766-032
Start Marketing Date : 2017-03-28
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65085-0071
Start Marketing Date : 2023-01-02
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : DRUG FOR FURTHER PROCESSING
NDC Package Code : 53069-1060
Start Marketing Date : 2014-02-18
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38217-0030
Start Marketing Date : 2014-02-18
End Marketing Date : 2030-12-31
Dosage Form (Strength) : POWDER (40kg/1)
Marketing Category : DRUG FOR FURTHER PROCESSING
A Droxidopa manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Droxidopa, including repackagers and relabelers. The FDA regulates Droxidopa manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Droxidopa 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 Droxidopa manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Droxidopa supplier is an individual or a company that provides Droxidopa active pharmaceutical ingredient (API) or Droxidopa finished formulations upon request. The Droxidopa suppliers may include Droxidopa API manufacturers, exporters, distributors and traders.
click here to find a list of Droxidopa 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 Droxidopa as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Droxidopa 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 Droxidopa 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 Droxidopa and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Droxidopa NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Droxidopa suppliers with NDC on PharmaCompass.
We have 8 companies offering Droxidopa
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