ChemWerth works in generic API development & supply, non-infringement patent strategy development and regulatory support.
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01 1ChemWerth Inc
02 1HRV Global Life Sciences
03 1Shanghai Minbiotech
04 1AstraZeneca
05 1Aurobindo Pharma Limited
06 1Beijing Sciecure Pharmaceutical
07 1Chia Tai Tianqing Pharmaceutical Group
08 1Emcure Pharmaceuticals
09 1GLAND PHARMA LIMITED
10 1Guangzhou Tosun Pharmaceutical
11 1Lianyungang Runzhong Pharmaceutical Co Ltd
12 1MSN Laboratories
13 1Maithri Drugs
14 1Trifarma
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02 6India
03 1Italy
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05 1United Kingdom
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01 8Active
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01 4Valid
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01 1WC-0226
02 1WC-0407
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01 114593-925
02 159651-476
03 161662-0001
04 170600-020
05 179290-0001
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ChemWerth works in generic API development & supply, non-infringement patent strategy development and regulatory support.
GDUFA
DMF Review : Reviewed
Rev. Date : 2015-07-10
Pay. Date : 2015-02-05
DMF Number : 28996
Submission : 2015-01-30
Status : Active
Type : II
Certificate Number : R0-CEP 2020-337 - Rev 00
Issue Date : 2023-02-14
Type : Chemical
Substance Number : 1520
Status : Valid
Shanghai Minbiotech is the leading producer of biopharmaceuticals and a variety of high-end generic & innovative drugs.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 34968
Submission : 2020-07-04
Status : Active
Type : II
Certificate Number : R0-CEP 2020-218 - Rev 00
Issue Date : 2022-05-19
Type : Chemical
Substance Number : 1520
Status : Valid
Date of Issue : 2024-02-12
Valid Till : 2027-02-11
Written Confirmation Number : WC-0407
Address of the Firm :
GDUFA
DMF Review : Reviewed
Rev. Date : 2019-07-31
Pay. Date : 2019-07-05
DMF Number : 32652
Submission : 2018-03-30
Status : Active
Type : II
Certificate Number : R0-CEP 2021-342 - Rev 01
Issue Date : 2023-05-22
Type : Chemical
Substance Number : 1520
Status : Valid
Date of Issue : 2022-09-30
Valid Till : 2025-07-02
Written Confirmation Number : WC-0226
Address of the Firm :
NDC Package Code : 14593-925
Start Marketing Date : 2023-12-22
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (15kg/15kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-12-18
Pay. Date : 2013-09-12
DMF Number : 19085
Submission : 2006-01-04
Status : Active
Type : II
GDUFA
DMF Review : Reviewed
Rev. Date : 2016-01-08
Pay. Date : 2015-09-28
DMF Number : 29814
Submission : 2015-09-28
Status : Active
Type : II
GDUFA
DMF Review : Reviewed
Rev. Date : 2015-05-20
Pay. Date : 2015-03-11
DMF Number : 29056
Submission : 2015-02-05
Status : Active
Type : II
Certificate Number : R1-CEP 2017-137 - Rev 00
Issue Date : 2023-07-27
Type : Chemical
Substance Number : 1520
Status : Valid
NDC Package Code : 61662-0001
Start Marketing Date : 2014-01-13
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2020-01-03
Pay. Date : 2019-08-27
DMF Number : 33288
Submission : 2019-08-05
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 11385
Submission : 1995-03-15
Status : Inactive
Type : II
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PharmaCompass offers a list of Foscarnet 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 Foscarnet Sodium manufacturer or Foscarnet Sodium supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Foscarnet Sodium manufacturer or Foscarnet Sodium supplier.
PharmaCompass also assists you with knowing the Foscarnet Sodium API Price utilized in the formulation of products. Foscarnet Sodium API Price is not always fixed or binding as the Foscarnet Sodium Price is obtained through a variety of data sources. The Foscarnet Sodium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Foscarnet Sodium Hexahydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Foscarnet Sodium Hexahydrate, including repackagers and relabelers. The FDA regulates Foscarnet Sodium Hexahydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Foscarnet Sodium Hexahydrate 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 Foscarnet Sodium Hexahydrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Foscarnet Sodium Hexahydrate supplier is an individual or a company that provides Foscarnet Sodium Hexahydrate active pharmaceutical ingredient (API) or Foscarnet Sodium Hexahydrate finished formulations upon request. The Foscarnet Sodium Hexahydrate suppliers may include Foscarnet Sodium Hexahydrate API manufacturers, exporters, distributors and traders.
click here to find a list of Foscarnet Sodium Hexahydrate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
We have 14 companies offering Foscarnet Sodium Hexahydrate
Get in contact with the supplier of your choice: