01 1Chemische Fabrik Berg
02 1Herbrand PharmaChemicals GmbH
03 1Macleods Pharmaceuticals Limited
04 1Roche Diagnostics GmbH
05 1Suzhou Ryway Biotech
06 1Blank
01 16-PROPYL-2-THIOURACIL
02 4PROPYLTHIOURACIL
03 1PROPYLTHIOURACIL USP
01 1China
02 3Germany
03 1India
04 1Blank
01 4Active
02 2Inactive
01 1Complete
02 5Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 16578
Submission : 2003-05-07
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 4928
Submission : 1983-03-22
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2015-07-06
Pay. Date : 2015-05-12
DMF Number : 29101
Submission : 2015-04-28
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 8377
Submission : 1990-01-15
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 40904
Submission : 2024-11-26
Status : Active
Type : II
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 8278
Submission : 1989-10-03
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
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PharmaCompass offers a list of Propylthiouracil 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 Propylthiouracil manufacturer or Propylthiouracil supplier for your needs.
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PharmaCompass also assists you with knowing the Propylthiouracil API Price utilized in the formulation of products. Propylthiouracil API Price is not always fixed or binding as the Propylthiouracil Price is obtained through a variety of data sources. The Propylthiouracil Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Tox21_300280 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tox21_300280, including repackagers and relabelers. The FDA regulates Tox21_300280 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tox21_300280 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 Tox21_300280 supplier is an individual or a company that provides Tox21_300280 active pharmaceutical ingredient (API) or Tox21_300280 finished formulations upon request. The Tox21_300280 suppliers may include Tox21_300280 API manufacturers, exporters, distributors and traders.
click here to find a list of Tox21_300280 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Tox21_300280 DMF (Drug Master File) is a document detailing the whole manufacturing process of Tox21_300280 active pharmaceutical ingredient (API) in detail. Different forms of Tox21_300280 DMFs exist exist since differing nations have different regulations, such as Tox21_300280 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Tox21_300280 DMF submitted to regulatory agencies in the US is known as a USDMF. Tox21_300280 USDMF includes data on Tox21_300280's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Tox21_300280 USDMF is kept confidential to protect the manufacturer’s intellectual property.
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