01 3Patheon
01 3U.S.A
01 3Blank
01 3Blank
01 3Blank
01 3Blank
01 3Blank
01 168225-049
02 168225-050
03 168225-104
01 3Blank
NDC Package Code : 68225-049
Start Marketing Date : 2008-08-25
End Marketing Date : 2025-12-31
Dosage Form (Strength) : INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION (0.4mg/1)
Marketing Category : DRUG FOR FURTHER PROCESSING
NDC Package Code : 68225-050
Start Marketing Date : 2008-08-25
End Marketing Date : 2025-12-31
Dosage Form (Strength) : INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION (0.6mg/1)
Marketing Category : DRUG FOR FURTHER PROCESSING
NDC Package Code : 68225-104
Start Marketing Date : 2019-08-02
End Marketing Date : 2025-12-31
Dosage Form (Strength) : INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION (125ug/.25mL)
Marketing Category : DRUG FOR FURTHER PROCESSING
100
PharmaCompass offers a list of Semaxanib 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 Semaxanib manufacturer or Semaxanib supplier for your needs.
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A Su 5416 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Su 5416, including repackagers and relabelers. The FDA regulates Su 5416 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Su 5416 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 Su 5416 supplier is an individual or a company that provides Su 5416 active pharmaceutical ingredient (API) or Su 5416 finished formulations upon request. The Su 5416 suppliers may include Su 5416 API manufacturers, exporters, distributors and traders.
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