01 1Quimica Sintetica S.A.
01 1Tianeptine Sodium
01 1Spain
NDC Package Code : 53069-0940
Start Marketing Date : 2008-12-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Tianeptine Sodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tianeptine Sodium, including repackagers and relabelers. The FDA regulates Tianeptine Sodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tianeptine Sodium API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Tianeptine Sodium manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tianeptine Sodium supplier is an individual or a company that provides Tianeptine Sodium active pharmaceutical ingredient (API) or Tianeptine Sodium finished formulations upon request. The Tianeptine Sodium suppliers may include Tianeptine Sodium API manufacturers, exporters, distributors and traders.
click here to find a list of Tianeptine Sodium suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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 Tianeptine Sodium as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Tianeptine Sodium 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 Tianeptine Sodium 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 Tianeptine Sodium and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Tianeptine Sodium NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Tianeptine Sodium suppliers with NDC on PharmaCompass.
We have 1 companies offering Tianeptine Sodium
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