01 1Apicore US LLC
02 1DARMERICA, LLC
03 2F.I.S. FABBRICA ITALIANA SINTETICI S.P.A.
01 3PROCARBAZINE HYDROCHLORIDE
02 1Procarbazine HCl
01 1India
02 2Italy
03 1U.S.A
NDC Package Code : 14096-128
Start Marketing Date : 2010-05-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 71052-290
Start Marketing Date : 2021-09-08
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (5g/5g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 48087-0050
Start Marketing Date : 2010-04-14
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 48087-0085
Start Marketing Date : 2010-04-14
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Procarbazine Hydrochloride 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 Procarbazine Hydrochloride manufacturer or Procarbazine Hydrochloride supplier for your needs.
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PharmaCompass also assists you with knowing the Procarbazine Hydrochloride API Price utilized in the formulation of products. Procarbazine Hydrochloride API Price is not always fixed or binding as the Procarbazine Hydrochloride Price is obtained through a variety of data sources. The Procarbazine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Matulane (TN) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Matulane (TN), including repackagers and relabelers. The FDA regulates Matulane (TN) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Matulane (TN) API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Matulane (TN) supplier is an individual or a company that provides Matulane (TN) active pharmaceutical ingredient (API) or Matulane (TN) finished formulations upon request. The Matulane (TN) suppliers may include Matulane (TN) API manufacturers, exporters, distributors and traders.
click here to find a list of Matulane (TN) 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 Matulane (TN) as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Matulane (TN) 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 Matulane (TN) 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 Matulane (TN) and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Matulane (TN) NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Matulane (TN) suppliers with NDC on PharmaCompass.
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