DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 1Dr. Reddy's Laboratories Limited
02 1Dr.Reddy's Laboratories Limited
03 1Granules India Ltd
04 1Hetero Labs Limited
05 3MSN Laboratories Private Limited
06 1Natco Pharma Limited
07 1Shandong Lixin Pharmaceutical Co., Ltd.
08 1Sterling Pharma Solutions Limited
09 1Suzhou Lixin Pharmaceutical Co., Ltd.
10 3TAPI Croatia Industries Ltd.
11 1VALARY LAB PRIVATE LIMITED
01 1NILOTINIB HYDROCHLORIDE
02 1NILOTINIB HYDROCHLORIDE ANHYDROUS
03 1NILOTINIB TARTRATE
04 2Nilotinib
05 1Nilotinib Fumarate
06 2Nilotinib Hydrochloride
07 1Nilotinib Hydrochloride (Monohydrate)
08 1Nilotinib Hydrochloride Dihydrate
09 3Nilotinib Hydrochloride Monohydrate
10 1Nilotinib Hydrochloride Sesquihydrate
11 1nILOTINIB HYDROCHLORIDE MONOHYDRATE
01 2China
02 8India
03 1United Kingdom
04 4Blank
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
NILOTINIB HYDROCHLORIDE ANHYDROUS
NDC Package Code : 55111-979
Start Marketing Date : 2015-12-31
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
NILOTINIB HYDROCHLORIDE MONOHYDRATE
NDC Package Code : 62207-984
Start Marketing Date : 2022-09-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (600g/600g)
Marketing Category : BULK INGREDIENT
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
NILOTINIB HYDROCHLORIDE MONOHYDRATE
NDC Package Code : 71796-047
Start Marketing Date : 2022-07-08
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 54893-0069
Start Marketing Date : 2018-01-22
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NILOTINIB HYDROCHLORIDE MONOHYDRATE
NDC Package Code : 54893-0075
Start Marketing Date : 2018-03-29
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NILOTINIB HYDROCHLORIDE MONOHYDRATE
NDC Package Code : 50384-6700
Start Marketing Date : 2023-07-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (350kg/350kg)
Marketing Category : BULK INGREDIENT
NILOTINIB HYDROCHLORIDE MONOHYDRATE
NDC Package Code : 29930-008
Start Marketing Date : 2022-10-31
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NILOTINIB HYDROCHLORIDE ANHYDROUS
NDC Package Code : 11722-019
Start Marketing Date : 2010-04-23
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
NDC Package Code : 11722-070
Start Marketing Date : 2019-08-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
NDC Package Code : 11722-075
Start Marketing Date : 2024-02-07
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
A Nilotinib hydrochloride anhydrous manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nilotinib hydrochloride anhydrous, including repackagers and relabelers. The FDA regulates Nilotinib hydrochloride anhydrous manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nilotinib hydrochloride anhydrous 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 Nilotinib hydrochloride anhydrous manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Nilotinib hydrochloride anhydrous supplier is an individual or a company that provides Nilotinib hydrochloride anhydrous active pharmaceutical ingredient (API) or Nilotinib hydrochloride anhydrous finished formulations upon request. The Nilotinib hydrochloride anhydrous suppliers may include Nilotinib hydrochloride anhydrous API manufacturers, exporters, distributors and traders.
click here to find a list of Nilotinib hydrochloride anhydrous 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 Nilotinib hydrochloride anhydrous as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Nilotinib hydrochloride anhydrous 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 Nilotinib hydrochloride anhydrous 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 Nilotinib hydrochloride anhydrous and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Nilotinib hydrochloride anhydrous NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Nilotinib hydrochloride anhydrous suppliers with NDC on PharmaCompass.
We have 7 companies offering Nilotinib hydrochloride anhydrous
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