01 1Zhejiang Ruibang Laboratories
01 1Thiostrepton
01 1China
NDC Package Code : 66507-7011
Start Marketing Date : 2017-12-04
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (0.5kg/.5kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Thiostrepton 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 Thiostrepton manufacturer or Thiostrepton supplier for your needs.
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A Panolog Cream (Veterinary) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Panolog Cream (Veterinary), including repackagers and relabelers. The FDA regulates Panolog Cream (Veterinary) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Panolog Cream (Veterinary) API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Panolog Cream (Veterinary) supplier is an individual or a company that provides Panolog Cream (Veterinary) active pharmaceutical ingredient (API) or Panolog Cream (Veterinary) finished formulations upon request. The Panolog Cream (Veterinary) suppliers may include Panolog Cream (Veterinary) 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 Panolog Cream (Veterinary) as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Panolog Cream (Veterinary) 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 Panolog Cream (Veterinary) 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 Panolog Cream (Veterinary) and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Panolog Cream (Veterinary) NDC to their finished compounded human drug products, they may choose to do so.
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