01 1Curia Italy S.r.l.
02 1Erregierre SpA
03 1SICOR Societa' Italiana Corticosteroidi s.r.l.
04 1Societa Italiana Medicinali Scandicci S.I.M.S., SrL
01 1TICLOPIDINE HYDROCHLORIDE
02 1Ticlopidine HCl
03 2Ticlopidine Hydrochloride
01 3Italy
02 1U.S.A
NDC Package Code : 55486-1565
Start Marketing Date : 2012-06-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49706-0331
Start Marketing Date : 2010-01-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 48292-0033
Start Marketing Date : 2015-02-13
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 12660-0501
Start Marketing Date : 1979-02-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Ticlopidine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ticlopidine, including repackagers and relabelers. The FDA regulates Ticlopidine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ticlopidine 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 Ticlopidine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ticlopidine supplier is an individual or a company that provides Ticlopidine active pharmaceutical ingredient (API) or Ticlopidine finished formulations upon request. The Ticlopidine suppliers may include Ticlopidine API manufacturers, exporters, distributors and traders.
click here to find a list of Ticlopidine 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 Ticlopidine as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Ticlopidine 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 Ticlopidine 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 Ticlopidine and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Ticlopidine NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Ticlopidine suppliers with NDC on PharmaCompass.
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