Zhejiang Hengkang Pharm Group is a dynamic pharmaceutical entity, spanning drug research, large-scale production, and global marketing.
01 1Zhejiang Hengkang Pharmaceutical
02 1Transo-Pharm USA LLC
03 1Metrochem API Private Limited
04 1Egis Pharmaceuticals PLC
05 1Shandong Chenghui Shuangda Pharmaceutical
06 1Jinan Tantu Chemicals
07 1Shandong Loncom Pharmaceutical
08 1TAPI Technology & API Services
09 1Aurobindo Pharma Limited
10 1Beijing Hope Pharmaceutical
11 1Beijing Sjar Technology Development
12 1Changzhou Pharmaceutical Factory
13 1Crystal Pharmaceutical
14 1Curia
15 1Hebi Xinhe Pharmaceutical
16 1Hetero Drugs
17 1Lee Pharma
18 1MSN Laboratories
19 1Morepen Laboratories
20 1Natco Pharma
21 1Optimus Pharma
22 1Sichuan Gowell Pharmaceutical
23 1Sichuan Qingmu Pharmaceutical
24 1Suzhou Biosyntech
25 1Viatris
26 1Zhejiang Tianyu Pharmaceutical Co., Ltd
27 1Blank
01 13China
02 1Hungary
03 8India
04 1Israel
05 3U.S.A
06 1Blank
01 9Active
02 18Blank
01 27Blank
01 27Blank
01 27Blank
Zhejiang Hengkang Pharm Group is a dynamic pharmaceutical entity, spanning drug research, large-scale production, and global marketing.
Metrochem has been delivering customized volume & quality products to customers across the world, taking utmost care of their needs.
Egis is a Hungarian generic pharma company with 110 years history. Our activities incorporate all areas of the pharma value chain.
China's leading API and intermediate manufacturer, offering CMO/CDMO services and exports to 70+ countries, enhancing global health.
Jinan Tantu Chemicals offers customized R&D services & production of small molecule APIs & pharmaceutical intermediates.
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
GDUFA
DMF Review : Reviewed
Rev. Date : 2023-07-17
Pay. Date : 2023-04-25
DMF Number : 38153
Submission : 2023-03-26
Status : Active
Type : II
NDC Package Code : 14501-0111
Start Marketing Date : 2023-03-26
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 : 40344
Submission : 2024-08-19
Status : Active
Type : II
GDUFA
DMF Review : Reviewed
Rev. Date : 2023-04-24
Pay. Date : 2023-02-21
DMF Number : 38095
Submission : 2023-02-22
Status : Active
Type : II
NDC Package Code : 59651-788
Start Marketing Date : 2023-12-25
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2022-08-16
Pay. Date : 2022-06-15
DMF Number : 37149
Submission : 2022-06-01
Status : Active
Type : II
NDC Package Code : 65089-0067
Start Marketing Date : 2024-03-22
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 40355
Submission : 2024-08-28
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 38427
Submission : 2023-06-15
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 38051
Submission : 2023-02-09
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 39581
Submission : 2024-03-12
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 : Reviewed
Rev. Date : 2023-07-05
Pay. Date : 2023-05-15
DMF Number : 38344
Submission : 2023-05-20
Status : Active
Type : II
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A Upadacitinib manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Upadacitinib, including repackagers and relabelers. The FDA regulates Upadacitinib manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Upadacitinib 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 Upadacitinib supplier is an individual or a company that provides Upadacitinib active pharmaceutical ingredient (API) or Upadacitinib finished formulations upon request. The Upadacitinib suppliers may include Upadacitinib API manufacturers, exporters, distributors and traders.
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