TransoPharm USA works in the Sourcing and Management of Active Pharmaceutical Ingredients.
01 1Transo-Pharm USA LLC
02 1ChemWerth Inc
03 1Dr. Reddy's Laboratories
04 1Jai Radhe Sales
05 1Cilag AG
06 1Divis Laboratories
07 1Fuan Pharmaceutical
08 1GLAND PHARMA LIMITED
09 1JPN Pharma
10 1Recordati
11 1Shanghai Ziyuan Pharmaceutical
12 1Sms Lifesciences
13 1Sun Pharmaceutical Industries Limited
14 1Trifarma
01 2China
02 7India
03 2Italy
04 1Switzerland
05 2U.S.A
01 5Active
02 4Inactive
03 5Blank
01 14Blank
01 14Blank
01 1WC-0067
02 1WC-0168
03 1WC-0181
04 1WC-0427A3-4
05 10Blank
ChemWerth works in generic API development & supply, non-infringement patent strategy development and regulatory support.
GDUFA
DMF Review : Reviewed
Rev. Date : 2023-05-03
Pay. Date : 2023-03-30
DMF Number : 37565
Submission : 2023-03-20
Status : Active
Type : II
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Date of Issue : 2022-06-17
Valid Till : 2025-07-07
Written Confirmation Number : WC-0067
Address of the Firm :
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 19455
Submission : 2006-05-25
Status : Active
Type : II
Date of Issue : 2022-08-08
Valid Till : 2025-07-14
Written Confirmation Number : WC-0168
Address of the Firm :
GDUFA
DMF Review : Reviewed
Rev. Date : 2017-06-16
Pay. Date : 2017-05-23
DMF Number : 17333
Submission : 2004-04-26
Status : Active
Type : II
GDUFA
DMF Review : Reviewed
Rev. Date : 2019-06-09
Pay. Date : 2019-04-24
DMF Number : 33756
Submission : 2019-04-29
Status : Active
Type : II
Date of Issue : 2022-08-04
Valid Till : 2025-03-04
Written Confirmation Number : WC-0427A3-4
Address of the Firm :
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 18806
Submission : 2005-09-25
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 16899
Submission : 2003-10-08
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 20970
Submission : 2007-10-24
Status : Inactive
Type : II
A Fosphenytoin Sodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fosphenytoin Sodium, including repackagers and relabelers. The FDA regulates Fosphenytoin Sodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fosphenytoin Sodium 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 Fosphenytoin Sodium manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Fosphenytoin Sodium supplier is an individual or a company that provides Fosphenytoin Sodium active pharmaceutical ingredient (API) or Fosphenytoin Sodium finished formulations upon request. The Fosphenytoin Sodium suppliers may include Fosphenytoin Sodium API manufacturers, exporters, distributors and traders.
click here to find a list of Fosphenytoin Sodium suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
We have 14 companies offering Fosphenytoin Sodium
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?