01 1SALICYLATES & CHEMICALS PRIVATE LIMITED
01 1BENZOPHENONE
01 1India
NDC Package Code : 76107-125
Start Marketing Date : 2018-09-18
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 Benzophenone 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 Benzophenone manufacturer or Benzophenone supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Benzophenone manufacturer or Benzophenone supplier.
PharmaCompass also assists you with knowing the Benzophenone API Price utilized in the formulation of products. Benzophenone API Price is not always fixed or binding as the Benzophenone Price is obtained through a variety of data sources. The Benzophenone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A DIPHENHYDRAMINE IMPURITY E manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DIPHENHYDRAMINE IMPURITY E, including repackagers and relabelers. The FDA regulates DIPHENHYDRAMINE IMPURITY E manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DIPHENHYDRAMINE IMPURITY E 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 DIPHENHYDRAMINE IMPURITY E supplier is an individual or a company that provides DIPHENHYDRAMINE IMPURITY E active pharmaceutical ingredient (API) or DIPHENHYDRAMINE IMPURITY E finished formulations upon request. The DIPHENHYDRAMINE IMPURITY E suppliers may include DIPHENHYDRAMINE IMPURITY E API manufacturers, exporters, distributors and traders.
click here to find a list of DIPHENHYDRAMINE IMPURITY E 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 DIPHENHYDRAMINE IMPURITY E as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for DIPHENHYDRAMINE IMPURITY E 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 DIPHENHYDRAMINE IMPURITY E 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 DIPHENHYDRAMINE IMPURITY E and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a DIPHENHYDRAMINE IMPURITY E NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of DIPHENHYDRAMINE IMPURITY E suppliers with NDC on PharmaCompass.
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