01 1Zhejiang Ruibang Laboratories
01 1China
01 1Active
01 1Blank
01 1Blank
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 15158
Submission : 2000-11-22
Status : Active
Type : II
NDC Package Code : 66507-7011
Start Marketing Date : 2003-01-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Thiostrepton manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Thiostrepton, including repackagers and relabelers. The FDA regulates Thiostrepton manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Thiostrepton 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 Thiostrepton supplier is an individual or a company that provides Thiostrepton active pharmaceutical ingredient (API) or Thiostrepton finished formulations upon request. The Thiostrepton suppliers may include Thiostrepton API manufacturers, exporters, distributors and traders.
click here to find a list of Thiostrepton suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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