01 1Srikem Laboratories Pvt. Ltd.
01 1Umifenovir Hydrochloride Monohydrate
01 1India
UMIFENOVIR HYDROCHLORIDE MONOHYDRATE
NDC Package Code : 13746-120
Start Marketing Date : 2021-11-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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A umifenovir hydrochloride monohydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of umifenovir hydrochloride monohydrate, including repackagers and relabelers. The FDA regulates umifenovir hydrochloride monohydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. umifenovir hydrochloride monohydrate 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 umifenovir hydrochloride monohydrate supplier is an individual or a company that provides umifenovir hydrochloride monohydrate active pharmaceutical ingredient (API) or umifenovir hydrochloride monohydrate finished formulations upon request. The umifenovir hydrochloride monohydrate suppliers may include umifenovir hydrochloride monohydrate 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 umifenovir hydrochloride monohydrate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for umifenovir hydrochloride monohydrate 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 umifenovir hydrochloride monohydrate 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 umifenovir hydrochloride monohydrate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a umifenovir hydrochloride monohydrate NDC to their finished compounded human drug products, they may choose to do so.
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