01 1DISHMAN CARBOGEN AMCIS LIMITED
02 1Professional Compounding Centers of America dba PCCA
03 1Trifarma S.p.A
01 2THIORIDAZINE HYDROCHLORIDE
02 1Thioridazine Hydrochloride
01 1India
02 1Italy
03 1United Kingdom
NDC Package Code : 61876-0075
Start Marketing Date : 2016-12-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-1928
Start Marketing Date : 2013-06-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 46204-0006
Start Marketing Date : 2012-05-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Thioridazine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Thioridazine Hydrochloride, including repackagers and relabelers. The FDA regulates Thioridazine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Thioridazine Hydrochloride 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 Thioridazine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Thioridazine Hydrochloride supplier is an individual or a company that provides Thioridazine Hydrochloride active pharmaceutical ingredient (API) or Thioridazine Hydrochloride finished formulations upon request. The Thioridazine Hydrochloride suppliers may include Thioridazine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Thioridazine Hydrochloride 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 Thioridazine Hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Thioridazine Hydrochloride 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 Thioridazine Hydrochloride 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 Thioridazine Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Thioridazine Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Thioridazine Hydrochloride suppliers with NDC on PharmaCompass.
We have 3 companies offering Thioridazine Hydrochloride
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