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01 1Dr.Reddy's Laboratories Limited

02 1Aurobindo Pharma Limited

03 1DARMERICA, LLC

04 2F.I.S. FABBRICA ITALIANA SINTETICI S.P.A.

05 1Formosa Laboratories, Inc.

06 1Hetero Labs Limited

07 1Hubei Biocause Heilen Pharmaceutical Co., Ltd

08 1LAURUS LABS LIMITED

09 1Laurus Labs Limited

10 2MSN Laboratories Private Limited

11 1Natco Pharma Limited

12 1Pliva Hrvatska d.o.o.

13 2SHILPA PHARMA LIFESCIENCES LIMITED

14 1SUN PHARMACEUTICAL INDUSTRIES, INC.

15 1Sterling Pharma Solutions Limited

16 1TAPI Croatia Industries Ltd.

17 1Valary Lab Private Limited

18 1zhejiang jiuzhou pharmaceutical Co., Ltd.

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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.

IMATINIB MESYLATE

NDC Package Code : 55111-939

Start Marketing Date : 2011-03-30

End Marketing Date : 2024-12-31

Dosage Form (Strength) : POWDER (1kg/kg)

Marketing Category : BULK INGREDIENT

Dr Reddy Company Banner

02

Medizin 2025
Not Confirmed
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Medizin 2025
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IMATINIB MESYLATE

NDC Package Code : 48087-0121

Start Marketing Date : 2018-12-20

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (1kg/kg)

Marketing Category : BULK INGREDIENT

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03

Medizin 2025
Not Confirmed
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Medizin 2025
Not Confirmed

IMATINIB

NDC Package Code : 48087-0143

Start Marketing Date : 2018-12-20

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (1kg/kg)

Marketing Category : BULK INGREDIENT

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04

Medizin 2025
Not Confirmed
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05

Medizin 2025
Not Confirmed
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06

Medizin 2025
Not Confirmed
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07

Medizin 2025
Not Confirmed
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08

Medizin 2025
Not Confirmed
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Medizin 2025
Not Confirmed

IMATINIB

NDC Package Code : 11722-080

Start Marketing Date : 2024-05-13

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (1kg/kg)

Marketing Category : BULK INGREDIENT

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09

Medizin 2025
Not Confirmed
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10

TAPI Croatia Industries Ltd.

Country
Medizin 2025
Not Confirmed
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TAPI Croatia Industries Ltd.

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Medizin 2025
Not Confirmed

IMATINIB MESYLATE

NDC Package Code : 11722-052

Start Marketing Date : 2011-12-09

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (100kg/100kg)

Marketing Category : BULK INGREDIENT

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Imatinib Mesylate Manufacturers

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

Imatinib Mesylate Suppliers

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

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

Imatinib Mesylate NDC

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 Imatinib Mesylate as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for Imatinib Mesylate API and other APIs are published in this directory by the FDA.

Unfinished drugs

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 Imatinib Mesylate 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.

Compounded drug products

The NDC directory also contains data on finished compounded human drug products that contain Imatinib Mesylate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Imatinib Mesylate NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of Imatinib Mesylate suppliers with NDC on PharmaCompass.

Imatinib Mesylate Manufacturers | Traders | Suppliers

Imatinib Mesylate 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.