TAPI offers customized CDMO Solutions for API development and manufacturing services.
01 2TAPI Technology & API Services
02 1Alembic Pharmaceuticals Limited
03 1Beijing Huikang Boyuan Chemical Tech
04 1Changzhou Pharmaceutical Factory
05 1Fuxin Long Rui Pharmaceutical
06 1Laurus Labs
07 1Lupin Ltd
08 1Viatris
01 5SOFOSBUVIR
02 1SOFOSBUVIR (AMORPHOUS)
03 1SOFOSBUVIR 1213
04 1SOFOSBUVIR 1613
05 1SOFOSBUVIR PREMIX
01 3China
02 3India
03 2Israel
04 1U.S.A
01 8Active
02 1Inactive
01 5Complete
02 4Blank
GDUFA
DMF Review : Complete
Rev. Date : 2017-07-18
Pay. Date : 2017-05-18
DMF Number : 31736
Submission : 2017-06-28
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2017-08-04
Pay. Date : 2017-05-25
DMF Number : 31737
Submission : 2017-07-04
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 32075
Submission : 2017-09-30
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 28919
Submission : 2014-12-24
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2018-01-24
Pay. Date : 2017-09-15
DMF Number : 32048
Submission : 2017-09-06
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 33487
Submission : 2019-07-07
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2017-12-15
Pay. Date : 2017-10-23
DMF Number : 32068
Submission : 2017-11-10
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 31511
Submission : 2017-04-14
Status : Inactive
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2017-10-27
Pay. Date : 2017-08-23
DMF Number : 31272
Submission : 2017-09-01
Status : Active
Type : II
A Sofosbuvir manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sofosbuvir, including repackagers and relabelers. The FDA regulates Sofosbuvir manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sofosbuvir 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 Sofosbuvir manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sofosbuvir supplier is an individual or a company that provides Sofosbuvir active pharmaceutical ingredient (API) or Sofosbuvir finished formulations upon request. The Sofosbuvir suppliers may include Sofosbuvir API manufacturers, exporters, distributors and traders.
click here to find a list of Sofosbuvir suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Sofosbuvir DMF (Drug Master File) is a document detailing the whole manufacturing process of Sofosbuvir active pharmaceutical ingredient (API) in detail. Different forms of Sofosbuvir DMFs exist exist since differing nations have different regulations, such as Sofosbuvir USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Sofosbuvir DMF submitted to regulatory agencies in the US is known as a USDMF. Sofosbuvir USDMF includes data on Sofosbuvir's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Sofosbuvir USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Sofosbuvir suppliers with USDMF on PharmaCompass.
We have 8 companies offering Sofosbuvir
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