TransoPharm USA works in the Sourcing and Management of Active Pharmaceutical Ingredients.
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01 1Transo-Pharm USA LLC
02 1ChemWerth Inc
03 1Jai Radhe Sales
04 1JPN Pharma
05 1Alchymars ICM SM
06 1Cilag AG
07 1Divis Laboratories
08 1Fuan Pharmaceutical
09 1GLAND PHARMA LIMITED
10 1Recordati
11 1Shanghai Ziyuan Pharmaceutical
12 1Sms Lifesciences
13 1Sun Pharmaceutical Industries Limited
14 1Trifarma
15 1Blank
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01 2China
02 7India
03 2Italy
04 1Switzerland
05 2U.S.A
06 1Blank
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01 5Active
02 4Inactive
03 6Blank
01 15Blank
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01 15Blank
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01 1WC-0168
02 1WC-0181
03 1WC-0427A3-4
04 12Blank
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01 15Blank
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01 114998-0018
02 152952-005
03 182019-0002
04 12Blank
01 15Blank
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
JPN Pharma offers excellence in API manufacturing through precision, innovation & quality, delivering solutions to the pharma industry
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 : 2021-02-09
Pay. Date : 2020-03-05
DMF Number : 32816
Submission : 2018-08-08
Status : Active
Type : II
NDC Package Code : 52952-005
Start Marketing Date : 2017-11-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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 : 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 : N/A
Rev. Date :
Pay. Date :
DMF Number : 20970
Submission : 2007-10-24
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 16899
Submission : 2003-10-08
Status : Inactive
Type : II
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PharmaCompass offers a list of Fosphenytoin Sodium 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 Fosphenytoin Sodium manufacturer or Fosphenytoin Sodium supplier for your needs.
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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.
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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: