01 1Apicore Pharmaceuticals Private Limited
02 1Ash Stevens LLC
03 1MSN Laboratories Private Limited
04 1Zhejiang Lepu Pharmaceutical Co., Ltd.
01 1PONATINIB HYDROCHLORIDE
02 3Ponatinib Hydrochloride
01 1China
02 2India
03 1U.S.A
NDC Package Code : 42973-242
Start Marketing Date : 2017-12-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 48957-0070
Start Marketing Date : 2012-12-14
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 54893-0124
Start Marketing Date : 2022-12-30
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 68578-0016
Start Marketing Date : 2022-10-13
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
A Ponatinib Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ponatinib Hydrochloride, including repackagers and relabelers. The FDA regulates Ponatinib Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ponatinib 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 Ponatinib Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ponatinib Hydrochloride supplier is an individual or a company that provides Ponatinib Hydrochloride active pharmaceutical ingredient (API) or Ponatinib Hydrochloride finished formulations upon request. The Ponatinib Hydrochloride suppliers may include Ponatinib Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Ponatinib 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 Ponatinib Hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Ponatinib 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 Ponatinib 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 Ponatinib Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Ponatinib Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Ponatinib Hydrochloride suppliers with NDC on PharmaCompass.
We have 4 companies offering Ponatinib Hydrochloride
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