Fujian Genohope Biotech is a leading provider of high-potency peptide APIs, offering GMP quality and worldwide delivery.
01 1Fujian Genohope Biotech Ltd.
01 1water
01 1China
Fujian Genohope Biotech is a leading provider of high-potency peptide APIs, offering GMP quality and worldwide delivery.
NDC Package Code : 84502-106
Start Marketing Date : 2025-05-06
End Marketing Date : 2026-12-31
Dosage Form (Strength) : INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION (1mL/mL)
Marketing Category : BULK INGREDIENT
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A Water for injection, sterile manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Water for injection, sterile, including repackagers and relabelers. The FDA regulates Water for injection, sterile manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Water for injection, sterile 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 Water for injection, sterile supplier is an individual or a company that provides Water for injection, sterile active pharmaceutical ingredient (API) or Water for injection, sterile finished formulations upon request. The Water for injection, sterile suppliers may include Water for injection, sterile 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 Water for injection, sterile as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Water for injection, sterile 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 Water for injection, sterile 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 Water for injection, sterile and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Water for injection, sterile NDC to their finished compounded human drug products, they may choose to do so.
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