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01 2Dr. Reddy's Laboratories

02 1Sichuan Elixir Pharmaceuticals

03 1Granules India Limited

04 2TAPI Technology & API Services

05 1Cipla

06 1F.I.S. Fabbrica Italiana Sintetici

07 1Hetero Drugs

08 1Hikma Pharmaceuticals

09 3MSN Laboratories

10 1Natco Pharma

11 1Shilpa Medicare

12 1Sichuan Xieli Pharmaceutical

13 1Sun Pharmaceutical Industries Limited

14 1Suzhou Lixin Pharmaceutical

15 1Teva Pharmaceutical Industries

16 2Zhejiang Jiuzhou Pharmaceutical

17 1Blank

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

GDUFA

DMF Review : Complete

Rev. Date : 2016-03-16

Pay. Date : 2016-02-04

DMF Number : 30088

Submission : 2015-12-31

Status : Active

Type : II

Dr Reddy Company Banner

02

Cosmoprof
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSichuan Elixir Pharmaceutical, a manufacturer of small molecule APIs & a CMO/CDMO service provider for anti-tumor characteristic APIs..

GDUFA

DMF Review : N/A

Rev. Date :

Pay. Date :

DMF Number : 39648

Submission : 2024-03-27

Status : Active

Type : II

Sichuan Elixir Pharmaceuticals

03

Cosmoprof
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothGranules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.

GDUFA

DMF Review : N/A

Rev. Date :

Pay. Date :

DMF Number : 37531

Submission : 2022-09-30

Status : Active

Type : II

Granules India

04

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothTAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.

GDUFA

DMF Review : Complete

Rev. Date : 2014-08-13

Pay. Date : 2014-03-19

DMF Number : 28102

Submission : 2014-07-15

Status : Active

Type : II

TAPI Company Banner

05

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

GDUFA

DMF Review : Complete

Rev. Date : 2022-09-15

Pay. Date : 2022-08-22

DMF Number : 37161

Submission : 2022-07-08

Status : Active

Type : II

Dr Reddy Company Banner

06

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothTAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.

GDUFA

DMF Review : Complete

Rev. Date : 2020-08-28

Pay. Date : 2020-05-13

DMF Number : 34874

Submission : 2020-07-14

Status : Active

Type : II

TAPI Company Banner

08

Cosmoprof
Not Confirmed

10

Cosmoprof
Not Confirmed

Nilotinib hydrochloride anhydrous Manufacturers

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.

Nilotinib hydrochloride anhydrous Suppliers

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.

Nilotinib hydrochloride anhydrous USDMF

A Nilotinib hydrochloride anhydrous DMF (Drug Master File) is a document detailing the whole manufacturing process of Nilotinib hydrochloride anhydrous active pharmaceutical ingredient (API) in detail. Different forms of Nilotinib hydrochloride anhydrous DMFs exist exist since differing nations have different regulations, such as Nilotinib hydrochloride anhydrous USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A Nilotinib hydrochloride anhydrous DMF submitted to regulatory agencies in the US is known as a USDMF. Nilotinib hydrochloride anhydrous USDMF includes data on Nilotinib hydrochloride anhydrous's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Nilotinib hydrochloride anhydrous USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of Nilotinib hydrochloride anhydrous suppliers with USDMF on PharmaCompass.

Nilotinib hydrochloride anhydrous Manufacturers | Traders | Suppliers

Nilotinib hydrochloride anhydrous Manufacturers, Traders, Suppliers 1
Inform the supplier about your product requirements, specifying if you need a product with particular monograph like EP (Ph. Eur.), USP, JP, BP, or any other quality. In addition, clarify whether you need hydrochloride (HCl), anhydricum, base, micronisatum or a specific level of purity. To find reputable suppliers, utilize the filters and select those certified by GMP, FDA, or any other certification as per your requirement.
For your convenience, we have listed synonyms and CAS numbers to help you find the best supplier. The use of synonyms and CAS numbers can be helpful in identifying potential suppliers, but it is crucial to note that they might not always indicate the exact same product. It is important to confirm the product details with the supplier before making a purchase to ensure that it meets your requirements.