Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
01 1Polpharma
02 1LGM Pharma
03 1Sichuan Elixir Pharmaceuticals
04 1Alembic Pharmaceuticals Limited
05 1Aurobindo Pharma Limited
06 1Aurore Life Sciences
07 2Guangdong Raffles PharmaTech Co Ltd
08 1Hangzhou Longshine Bio-Tech
09 1Hetero Drugs
10 2MSN Laboratories
11 1Parsian Pharamceutical
12 1Shenzhen Haorui
13 1Shenzhen HwaGen Pharmaceutical
14 1Viatris
15 1Zhejiang Multinpharma
16 1Blank
01 7China
02 6India
03 1Iran
04 1Poland
05 2U.S.A
06 1Blank
01 6Active
02 12Blank
01 18Blank
01 18Blank
01 1WC-0349
02 17Blank
Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 39561
Submission : 2024-06-19
Status : Active
Type : II
LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
Sichuan Elixir Pharmaceutical, a manufacturer of small molecule APIs & a CMO/CDMO service provider for anti-tumor characteristic APIs..
GDUFA
DMF Review : Reviewed
Rev. Date : 2022-10-18
Pay. Date : 2022-09-12
DMF Number : 37504
Submission : 2022-09-13
Status : Active
Type : II
NDC Package Code : 59651-710
Start Marketing Date : 2024-01-11
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 31589
Submission : 2017-03-31
Status : Active
Type : II
Date of Issue : 2022-09-02
Valid Till : 2025-05-05
Written Confirmation Number : WC-0349
Address of the Firm :
NDC Package Code : 54893-0062
Start Marketing Date : 2017-03-31
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2022-03-31
Pay. Date : 2022-01-06
DMF Number : 35525
Submission : 2020-12-31
Status : Active
Type : II
NDC Package Code : 54893-0062
Start Marketing Date : 2017-03-31
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 40493
Submission : 2024-09-29
Status : Active
Type : II
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 40250
Submission : 2024-08-23
Status : Active
Type : II
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A Trametinib Dimethyl Sulfoxide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Trametinib Dimethyl Sulfoxide, including repackagers and relabelers. The FDA regulates Trametinib Dimethyl Sulfoxide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Trametinib Dimethyl Sulfoxide 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 Trametinib Dimethyl Sulfoxide supplier is an individual or a company that provides Trametinib Dimethyl Sulfoxide active pharmaceutical ingredient (API) or Trametinib Dimethyl Sulfoxide finished formulations upon request. The Trametinib Dimethyl Sulfoxide suppliers may include Trametinib Dimethyl Sulfoxide API manufacturers, exporters, distributors and traders.
click here to find a list of Trametinib Dimethyl Sulfoxide suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
We have 15 companies offering Trametinib Dimethyl Sulfoxide
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