Qingmu Pharma: Patients first, FDA/CEP/US-DMF/US-VMF/ASMF APIs for Humans & Vets in 100+ countries.

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01 1Sichuan Qingmu Pharmaceutical
02 1Alembic Pharmaceuticals Limited
03 2Apicore
04 1Beijing Sjar Technology Development
05 1DEAFARMA
06 1Haohong (Qihe) Pharmaceutical Technology
07 1Hetero Drugs
08 1MSN Laboratories
09 1Protheragen
10 1Sai Phytoceuticals
11 1Signa S.A. de C.V.
12 1Sun Pharmaceutical Industries Limited
13 1Viatris
14 1Zhejiang Lepu Pharmaceutical
15 1Blank
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01 4China
02 7India
03 1Italy
04 1Mexico
05 2U.S.A
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01 4Active
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01 16Blank
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01 16Blank
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01 1WC-0110
02 1WC-0110A5
03 1WC-0349
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01 1Su173-64-ND
02 15Blank
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01 142973-242
02 148957-0070
03 154893-0124
04 168554-0186
05 168578-0016
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GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 37854
Submission : 2022-12-31
Status : Active
Type : II
Date of Issue : 2025-09-19
Valid Till : 2028-05-05
Written Confirmation Number : WC-0349
Address of the Firm :
NDC Package Code : 54893-0124
Start Marketing Date : 2022-12-30
End Marketing Date : 2027-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Gukjeon Co., Ltd.
Registration Date : 2025-09-24
Registration Number : Su173-64-ND
Manufacturer Name : MSN Laboratories Private Limited
Manufacturer Address : (Unit-ll) Sy. No. 50, 53, 53/A, 54 & 54/A, Kardanur (Village), Patancheru (Mandal), Sangareddy District, Telangana, Pincode: 502 300, India

GDUFA
DMF Review : Reviewed
Rev. Date : 2021-01-29
Pay. Date : 2020-11-27
DMF Number : 35413
Submission : 2020-12-16
Status : Active
Type : II

GDUFA
DMF Review : Reviewed
Rev. Date : 2022-07-22
Pay. Date : 2022-06-06
DMF Number : 32340
Submission : 2018-01-07
Status : Active
Type : II

GDUFA
DMF Review : Reviewed
Rev. Date : 2026-03-09
Pay. Date : 2026-01-29
DMF Number : 43274
Submission : 2026-01-29
Status : Active
Type : II


Date of Issue : 2021-04-15
Valid Till : 2022-02-07
Written Confirmation Number : WC-0110A5
Address of the Firm :

Date of Issue : 2025-11-27
Valid Till : 2028-07-02
Written Confirmation Number : WC-0110
Address of the Firm :
NDC Package Code : 42973-242
Start Marketing Date : 2017-12-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT



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PharmaCompass offers a list of Ponatinib API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Ponatinib manufacturer or Ponatinib supplier for your needs.
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A Ponatinib HCl manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ponatinib HCl, including repackagers and relabelers. The FDA regulates Ponatinib HCl manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ponatinib HCl API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Ponatinib HCl supplier is an individual or a company that provides Ponatinib HCl active pharmaceutical ingredient (API) or Ponatinib HCl finished formulations upon request. The Ponatinib HCl suppliers may include Ponatinib HCl API manufacturers, exporters, distributors and traders.
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We have 14 companies offering Ponatinib HCl
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