01 1Abhilasha Pharma Pvt. Ltd.
01 1Ascorbyl Palmitate
01 1India
NDC Package Code : 71277-0133
Start Marketing Date : 2018-05-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Ascorbyl Palmitate 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 Ascorbyl Palmitate manufacturer or Ascorbyl Palmitate supplier for your needs.
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PharmaCompass also assists you with knowing the Ascorbyl Palmitate API Price utilized in the formulation of products. Ascorbyl Palmitate API Price is not always fixed or binding as the Ascorbyl Palmitate Price is obtained through a variety of data sources. The Ascorbyl Palmitate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cetyl Ascorbate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cetyl Ascorbate, including repackagers and relabelers. The FDA regulates Cetyl Ascorbate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cetyl Ascorbate 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 Cetyl Ascorbate supplier is an individual or a company that provides Cetyl Ascorbate active pharmaceutical ingredient (API) or Cetyl Ascorbate finished formulations upon request. The Cetyl Ascorbate suppliers may include Cetyl Ascorbate 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 Cetyl Ascorbate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Cetyl Ascorbate 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 Cetyl Ascorbate 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 Cetyl Ascorbate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Cetyl Ascorbate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Cetyl Ascorbate suppliers with NDC on PharmaCompass.
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