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01 2Dr. Reddy's Laboratories

02 1Sichuan Elixir Pharmaceuticals

03 2Granules India Limited

04 2TAPI Technology & API Services

05 1ALP Pharm

06 1Alembic Pharmaceuticals Limited

07 1Aurobindo Pharma Limited

08 1Biocare Pharmaceutical

09 1Biocon

10 2Cdymax

11 3Cipla

12 1Deva Holding AS

13 1Hetero Drugs

14 1Hikma Pharmaceuticals

15 2Hubei Haosun Pharmaceutical Co., Ltd.

16 1Intas Pharmaceuticals

17 3MSN Laboratories

18 1Reliance Life Sciences Private Limited

19 1Sichuan Xieli Pharmaceutical

20 1Sun Pharmaceutical Industries Limited

21 1Zhejiang Hisun Pharmaceutical

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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 : 2018-10-11

Pay. Date : 2018-08-31

DMF Number : 32400

Submission : 2018-02-23

Status : Active

Type : II

Dr Reddy Company Banner

02

PharmaVenue
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 : 39646

Submission : 2024-03-27

Status : Active

Type : II

Sichuan Elixir Pharmaceuticals

03

PharmaVenue
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 : 35270

Submission : 2020-11-23

Status : Active

Type : II

Granules India

04

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothTAPI offers customized CDMO Solutions for API development and manufacturing services.

GDUFA

DMF Review : Complete

Rev. Date : 2017-05-10

Pay. Date : 2017-04-03

DMF Number : 31605

Submission : 2017-04-18

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 : N/A

Rev. Date :

Pay. Date :

DMF Number : 34676

Submission : 2020-03-12

Status : Active

Type : II

Dr Reddy Company Banner

06

PharmaVenue
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 : 38065

Submission : 2023-03-31

Status : Active

Type : II

Granules India

07

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothTAPI offers customized CDMO Solutions for API development and manufacturing services.

GDUFA

DMF Review : Complete

Rev. Date : 2018-03-20

Pay. Date : 2017-11-28

DMF Number : 32407

Submission : 2018-01-31

Status : Active

Type : II

TAPI Company Banner

10

PharmaVenue
Not Confirmed

Dasatinib Manufacturers

A Dasatinib manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dasatinib, including repackagers and relabelers. The FDA regulates Dasatinib manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dasatinib 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 Dasatinib manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

Dasatinib Suppliers

A Dasatinib supplier is an individual or a company that provides Dasatinib active pharmaceutical ingredient (API) or Dasatinib finished formulations upon request. The Dasatinib suppliers may include Dasatinib API manufacturers, exporters, distributors and traders.

click here to find a list of Dasatinib suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

Dasatinib USDMF

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

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

click here to find a list of Dasatinib suppliers with USDMF on PharmaCompass.

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.