Minakem delivers API, HPAPI, steroids & CDMO services for generics with FDA/GMP certification, regulatory know-how & proven success.
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02 1Transo-Pharm USA LLC
03 1HRV Global Life Sciences
04 1TAPI Technology & API Services
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11 1Hetero Drugs
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01 1229MF10183
02 1229MF10184
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01 1WC-0022
02 1WC-0066
03 1WC-0213
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01 1Su217-14-ND
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01 115894-0032
02 150370-0052
03 153104-7734
04 165267-501
05 165977-0104
06 167835-0013
07 172761-038
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Minakem delivers API, HPAPI, steroids & CDMO services for generics with FDA/GMP certification, regulatory know-how & proven success.
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
NDC Package Code : 15894-0032
Start Marketing Date : 2016-08-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-09-30
Pay. Date : 2013-07-08
DMF Number : 27253
Submission : 2013-07-24
Status : Active
Type : II
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-02-07
Pay. Date : 2012-12-26
DMF Number : 23824
Submission : 2010-07-19
Status : Active
Type : II
Registration Number : 229MF10183
Registrant's Address : Little Island Industrial Estate, Little Island, Co. Cork, Ireland
Initial Date of Registration : 2017-10-06
Latest Date of Registration :
NDC Package Code : 65267-501
Start Marketing Date : 2010-07-19
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Korea Janssen Co., Ltd.
Registration Date : 2011-10-28
Registration Number : Su217-14-ND
Manufacturer Name : Janssen Pharmaceutical Sciences Unlimited Company
Manufacturer Address : Little Island Industrial EST., Little Island, Co. Cork, Ireland_x000D_
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 39552
Submission : 2024-02-27
Status : Active
Type : II
GDUFA
DMF Review : Reviewed
Rev. Date : 2016-06-15
Pay. Date : 2015-11-02
DMF Number : 29841
Submission : 2015-12-08
Status : Active
Type : II
Date of Issue : 2023-07-03
Valid Till : 2025-07-02
Written Confirmation Number : WC-0213
Address of the Firm :
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 37479
Submission : 2022-09-23
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 26305
Submission : 2012-08-03
Status : Inactive
Type : II
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PharmaCompass offers a list of Rilpivirine Hydrochloride API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Rilpivirine Hydrochloride manufacturer or Rilpivirine Hydrochloride supplier for your needs.
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A Edurant manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Edurant, including repackagers and relabelers. The FDA regulates Edurant manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Edurant 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 Edurant manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Edurant supplier is an individual or a company that provides Edurant active pharmaceutical ingredient (API) or Edurant finished formulations upon request. The Edurant suppliers may include Edurant API manufacturers, exporters, distributors and traders.
click here to find a list of Edurant suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
We have 19 companies offering Edurant
Get in contact with the supplier of your choice: