Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
01 1Symbiotec Pharmalab Private Limited
02 1Henan Lihua Pharmaceutical Co Ltd
01 2Hydrocortisone Sodium Succinate
01 1China
02 1India
Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
HYDROCORTISONE SODIUM SUCCINATE
NDC Package Code : 22552-0007
Start Marketing Date : 2017-12-13
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
HYDROCORTISONE SODIUM SUCCINATE
NDC Package Code : 64958-0020
Start Marketing Date : 2007-04-06
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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A Flebocortid manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Flebocortid, including repackagers and relabelers. The FDA regulates Flebocortid manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Flebocortid 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 Flebocortid supplier is an individual or a company that provides Flebocortid active pharmaceutical ingredient (API) or Flebocortid finished formulations upon request. The Flebocortid suppliers may include Flebocortid 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 Flebocortid as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Flebocortid 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 Flebocortid 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 Flebocortid and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Flebocortid NDC to their finished compounded human drug products, they may choose to do so.
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