01 1Jiangsu Hansoh Pharmaceutical Group Co., Ltd.
02 1MSN Laboratories Private Limited
03 2ScinoPharm Taiwan Ltd.
04 3Teva Czech Industries s.r.o
01 5Pemetrexed
02 1Pemetrexed Diacid
03 1Pemetrexed Dipotassium Heptahydrate
01 1China
02 1India
03 3Israel
04 2Taiwan
NDC Package Code : 66529-0008
Start Marketing Date : 2014-12-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (10kg/10kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 54893-0063
Start Marketing Date : 2017-03-31
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65129-1366
Start Marketing Date : 2015-01-14
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65129-1366
Start Marketing Date : 2016-01-11
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 47848-026
Start Marketing Date : 2012-08-09
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 47848-026
Start Marketing Date : 2022-01-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 47848-026
Start Marketing Date : 2012-08-09
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Pemetrexed 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 Pemetrexed manufacturer or Pemetrexed supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Pemetrexed manufacturer or Pemetrexed supplier.
PharmaCompass also assists you with knowing the Pemetrexed API Price utilized in the formulation of products. Pemetrexed API Price is not always fixed or binding as the Pemetrexed Price is obtained through a variety of data sources. The Pemetrexed Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A ALIMTA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of ALIMTA, including repackagers and relabelers. The FDA regulates ALIMTA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. ALIMTA 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 ALIMTA manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A ALIMTA supplier is an individual or a company that provides ALIMTA active pharmaceutical ingredient (API) or ALIMTA finished formulations upon request. The ALIMTA suppliers may include ALIMTA API manufacturers, exporters, distributors and traders.
click here to find a list of ALIMTA 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 ALIMTA as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for ALIMTA 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 ALIMTA 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 ALIMTA and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a ALIMTA NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of ALIMTA suppliers with NDC on PharmaCompass.
We have 4 companies offering ALIMTA
Get in contact with the supplier of your choice:
