01 2Qingdao Biopeptek Co., Ltd.
01 1Noopept
02 1Omberacetam
01 2Blank
NDC Package Code : 73212-200
Start Marketing Date : 2025-12-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
NDC Package Code : 73212-202
Start Marketing Date : 2025-07-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
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A N-Phenylacetyl-L-Prolylglycine Ethyl Ester manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of N-Phenylacetyl-L-Prolylglycine Ethyl Ester, including repackagers and relabelers. The FDA regulates N-Phenylacetyl-L-Prolylglycine Ethyl Ester manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. N-Phenylacetyl-L-Prolylglycine Ethyl Ester 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 N-Phenylacetyl-L-Prolylglycine Ethyl Ester supplier is an individual or a company that provides N-Phenylacetyl-L-Prolylglycine Ethyl Ester active pharmaceutical ingredient (API) or N-Phenylacetyl-L-Prolylglycine Ethyl Ester finished formulations upon request. The N-Phenylacetyl-L-Prolylglycine Ethyl Ester suppliers may include N-Phenylacetyl-L-Prolylglycine Ethyl Ester 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 N-Phenylacetyl-L-Prolylglycine Ethyl Ester as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for N-Phenylacetyl-L-Prolylglycine Ethyl Ester 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 N-Phenylacetyl-L-Prolylglycine Ethyl Ester 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 N-Phenylacetyl-L-Prolylglycine Ethyl Ester and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a N-Phenylacetyl-L-Prolylglycine Ethyl Ester NDC to their finished compounded human drug products, they may choose to do so.
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