01 1BDR Lifesciences Private Limited
02 1Bidachem S.p.a.
03 2Formosa Laboratories, Inc.
04 1Hetero Labs Limited
05 1Hubei Humanwell Chengtian Pharmaceutical Co., Ltd.
06 1Jiangsu Hansoh Pharmaceutical Group Co., Ltd.
07 2MSN Laboratories Private Limited
08 3Olon S.p.A.
09 1Sicor de Mexico S.A. de C.V
01 1NINTEDANIB ESYLATE
02 1NINTEDANIB ESYLATE HEMIYDRATE
03 2Nintedanib
04 1Nintedanib (Base)
05 2Nintedanib Base
06 5Nintedanib Esylate
07 1Nintedanib esylate
01 2China
02 4India
03 4Italy
04 1Mexico
05 2Taiwan
NDC Package Code : 51869-0040
Start Marketing Date : 2014-10-14
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 66499-0061
Start Marketing Date : 2018-04-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 66499-0062
Start Marketing Date : 2018-04-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 66529-0015
Start Marketing Date : 2019-12-20
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 54893-0051
Start Marketing Date : 2016-09-23
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 54893-0059
Start Marketing Date : 2017-03-27
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17337-0092
Start Marketing Date : 2020-05-19
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17337-0093
Start Marketing Date : 2020-06-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17337-0329
Start Marketing Date : 2023-10-02
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 63592-7200
Start Marketing Date : 2016-07-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT
A Nintedanib manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nintedanib, including repackagers and relabelers. The FDA regulates Nintedanib manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nintedanib 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 Nintedanib manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Nintedanib supplier is an individual or a company that provides Nintedanib active pharmaceutical ingredient (API) or Nintedanib finished formulations upon request. The Nintedanib suppliers may include Nintedanib API manufacturers, exporters, distributors and traders.
click here to find a list of Nintedanib 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 Nintedanib as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Nintedanib 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 Nintedanib 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 Nintedanib and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Nintedanib NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Nintedanib suppliers with NDC on PharmaCompass.
We have 9 companies offering Nintedanib
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