Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
01 1Aarti Pharmalabs Limited
02 1Jiangsu Hengrui Pharmaceuticals Co., Ltd.
01 2Ifosfamide
01 1China
02 1India
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
NDC Package Code : 15308-0411
Start Marketing Date : 1990-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 57884-0006
Start Marketing Date : 2010-08-25
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Ifosfamide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ifosfamide, including repackagers and relabelers. The FDA regulates Ifosfamide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ifosfamide 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 Ifosfamide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ifosfamide supplier is an individual or a company that provides Ifosfamide active pharmaceutical ingredient (API) or Ifosfamide finished formulations upon request. The Ifosfamide suppliers may include Ifosfamide API manufacturers, exporters, distributors and traders.
click here to find a list of Ifosfamide 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 Ifosfamide as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Ifosfamide 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 Ifosfamide 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 Ifosfamide and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Ifosfamide NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Ifosfamide suppliers with NDC on PharmaCompass.
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