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 1COHANCE LIFESCIENCES LIMITED
03 1Formosa Laboratories, Inc.
04 1LUPIN MANUFACTURING SOLUTIONS LIMITED
05 1Siegfried St. Vulbas SAS
06 1Siegfried USA, LLC
01 5Ferric Citrate
02 1Ferric citrate
01 3India
02 2Switzerland
03 1Taiwan
Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
TETRAFERRIC TRICITRATE DECAHYDRATE
NDC Package Code : 58159-035
Start Marketing Date : 2019-10-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (35kg/35kg)
Marketing Category : BULK INGREDIENT
Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
NDC Package Code : 17511-124
Start Marketing Date : 2018-10-11
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1mg/mg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 66499-0069
Start Marketing Date : 2019-11-20
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 83786-001
Start Marketing Date : 2023-11-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
TETRAFERRIC TRICITRATE DECAHYDRATE
NDC Package Code : 0792-0046
Start Marketing Date : 2013-01-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
TETRAFERRIC TRICITRATE DECAHYDRATE
NDC Package Code : 65675-1114
Start Marketing Date : 2014-09-05
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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A Tetraferric tricitrate decahydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tetraferric tricitrate decahydrate, including repackagers and relabelers. The FDA regulates Tetraferric tricitrate decahydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tetraferric tricitrate decahydrate 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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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 Tetraferric tricitrate decahydrate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Tetraferric tricitrate decahydrate 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 Tetraferric tricitrate decahydrate 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 Tetraferric tricitrate decahydrate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Tetraferric tricitrate decahydrate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Tetraferric tricitrate decahydrate suppliers with NDC on PharmaCompass.
We have 5 companies offering Tetraferric tricitrate decahydrate
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