01 1BSP Pharmaceuticals
01 1Italy
01 1Blank
01 1Blank
01 1Blank
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01 143624-008
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NDC Package Code : 43624-008
Start Marketing Date : 2020-04-23
End Marketing Date : 2026-12-31
Dosage Form (Strength) : INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION (180mg/180mg)
Marketing Category : DRUG FOR FURTHER PROCESSING
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A Sacituzumab Govitecan manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sacituzumab Govitecan, including repackagers and relabelers. The FDA regulates Sacituzumab Govitecan manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sacituzumab Govitecan 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 Sacituzumab Govitecan supplier is an individual or a company that provides Sacituzumab Govitecan active pharmaceutical ingredient (API) or Sacituzumab Govitecan finished formulations upon request. The Sacituzumab Govitecan suppliers may include Sacituzumab Govitecan API manufacturers, exporters, distributors and traders.
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