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 1Trifarma S.p.A
01 1Tranylcypromine Sulfate
02 1Tranylcypromine sulfate
01 1India
02 1Italy
Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
NDC Package Code : 58159-082
Start Marketing Date : 2025-01-02
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (35kg/35kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 46204-0130
Start Marketing Date : 2017-12-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Tranylcypromine Sulfate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Tranylcypromine Sulfate manufacturer or Tranylcypromine Sulfate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Tranylcypromine Sulfate manufacturer or Tranylcypromine Sulfate supplier.
PharmaCompass also assists you with knowing the Tranylcypromine Sulfate API Price utilized in the formulation of products. Tranylcypromine Sulfate API Price is not always fixed or binding as the Tranylcypromine Sulfate Price is obtained through a variety of data sources. The Tranylcypromine Sulfate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Parnate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Parnate, including repackagers and relabelers. The FDA regulates Parnate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Parnate 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 Parnate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Parnate supplier is an individual or a company that provides Parnate active pharmaceutical ingredient (API) or Parnate finished formulations upon request. The Parnate suppliers may include Parnate API manufacturers, exporters, distributors and traders.
click here to find a list of Parnate 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 Parnate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Parnate 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 Parnate 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 Parnate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Parnate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Parnate suppliers with NDC on PharmaCompass.
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