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 1Porton Pharma Solutions Ltd
03 1Azico Biophore India Private Limited
04 1Henan Quanyu Pharmaceutical Co., Ltd.
05 1MSN Life Sciences Private Limited
06 1Medisca
07 1Saurav Chemicals Limited
01 1TIOPRONIN
02 6Tiopronin
01 2China
02 4India
03 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 : 58159-057
Start Marketing Date : 2017-11-09
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (35kg/35kg)
Marketing Category : BULK INGREDIENT
Porton Pharma Solutions: Value creation via innovation & discovery through technical platforms.
NDC Package Code : 75877-0004
Start Marketing Date : 2014-01-10
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 69575-4037
Start Marketing Date : 2021-12-16
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 83916-440
Start Marketing Date : 2024-01-05
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 38779-3299
Start Marketing Date : 2024-01-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 69766-033
Start Marketing Date : 2017-10-23
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 43235-0008
Start Marketing Date : 2018-09-10
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : DRUG FOR FURTHER PROCESSING
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PharmaCompass offers a list of Tiopronin 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 Tiopronin manufacturer or Tiopronin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Tiopronin manufacturer or Tiopronin supplier.
PharmaCompass also assists you with knowing the Tiopronin API Price utilized in the formulation of products. Tiopronin API Price is not always fixed or binding as the Tiopronin Price is obtained through a variety of data sources. The Tiopronin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Mucolysin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Mucolysin, including repackagers and relabelers. The FDA regulates Mucolysin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Mucolysin 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 Mucolysin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Mucolysin supplier is an individual or a company that provides Mucolysin active pharmaceutical ingredient (API) or Mucolysin finished formulations upon request. The Mucolysin suppliers may include Mucolysin API manufacturers, exporters, distributors and traders.
click here to find a list of Mucolysin 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 Mucolysin as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Mucolysin 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 Mucolysin 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 Mucolysin and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Mucolysin NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Mucolysin suppliers with NDC on PharmaCompass.
We have 7 companies offering Mucolysin
Get in contact with the supplier of your choice:
