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
01 1Propantheline Bromide
01 1India
Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
NDC Package Code : 58159-065
Start Marketing Date : 2018-12-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (35kg/35kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Propantheline Bromide 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 Propantheline Bromide manufacturer or Propantheline Bromide supplier for your needs.
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PharmaCompass also assists you with knowing the Propantheline Bromide API Price utilized in the formulation of products. Propantheline Bromide API Price is not always fixed or binding as the Propantheline Bromide Price is obtained through a variety of data sources. The Propantheline Bromide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Pro Banthine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Pro Banthine, including repackagers and relabelers. The FDA regulates Pro Banthine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Pro Banthine 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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A Pro Banthine supplier is an individual or a company that provides Pro Banthine active pharmaceutical ingredient (API) or Pro Banthine finished formulations upon request. The Pro Banthine suppliers may include Pro Banthine API manufacturers, exporters, distributors and traders.
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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 Pro Banthine as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Pro Banthine 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 Pro Banthine 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 Pro Banthine and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Pro Banthine NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Pro Banthine suppliers with NDC on PharmaCompass.
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