01 1Andhra Organics Limited.
02 1Hunan Xiangyikang Pharmaceutical
03 1Shanghai Ziyuan Pharmaceutical
04 1Southwest Synthetic Pharmaceutical
05 1Blank
01 3SULFADIAZINE
02 2SULFADIAZINE USP
01 3China
02 1India
03 1Blank
01 2Active
02 3Inactive
01 2Complete
02 3Blank
GDUFA
DMF Review : Complete
Rev. Date : 2024-08-21
Pay. Date : 2024-08-13
DMF Number : 38268
Submission : 2023-05-12
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2020-07-14
Pay. Date : 2020-06-19
DMF Number : 33237
Submission : 2018-12-13
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 8699
Submission : 1990-08-08
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 22692
Submission : 2009-04-02
Status : Inactive
Type : II
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3941
Submission : 1980-09-05
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 Sulfadiazine 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 Sulfadiazine manufacturer or Sulfadiazine supplier for your needs.
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A Trisulfapyrimidine, oral suspension manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Trisulfapyrimidine, oral suspension, including repackagers and relabelers. The FDA regulates Trisulfapyrimidine, oral suspension manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Trisulfapyrimidine, oral suspension 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 Trisulfapyrimidine, oral suspension supplier is an individual or a company that provides Trisulfapyrimidine, oral suspension active pharmaceutical ingredient (API) or Trisulfapyrimidine, oral suspension finished formulations upon request. The Trisulfapyrimidine, oral suspension suppliers may include Trisulfapyrimidine, oral suspension API manufacturers, exporters, distributors and traders.
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A Trisulfapyrimidine, oral suspension DMF (Drug Master File) is a document detailing the whole manufacturing process of Trisulfapyrimidine, oral suspension active pharmaceutical ingredient (API) in detail. Different forms of Trisulfapyrimidine, oral suspension DMFs exist exist since differing nations have different regulations, such as Trisulfapyrimidine, oral suspension USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Trisulfapyrimidine, oral suspension DMF submitted to regulatory agencies in the US is known as a USDMF. Trisulfapyrimidine, oral suspension USDMF includes data on Trisulfapyrimidine, oral suspension's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Trisulfapyrimidine, oral suspension USDMF is kept confidential to protect the manufacturer’s intellectual property.
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