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01 2RITODRINE HCL
02 1YUTOPAR (RITODRINE HCL) TABLETS & INJECTION FORMS,OLST,HOLLAND
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01 3Inactive
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USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3490
Submission : 1979-03-06
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 6264
Submission : 1986-04-14
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 4527
Submission : 1982-04-26
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
A Ritodrine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ritodrine, including repackagers and relabelers. The FDA regulates Ritodrine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ritodrine 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 Ritodrine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ritodrine supplier is an individual or a company that provides Ritodrine active pharmaceutical ingredient (API) or Ritodrine finished formulations upon request. The Ritodrine suppliers may include Ritodrine API manufacturers, exporters, distributors and traders.
click here to find a list of Ritodrine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Ritodrine DMF (Drug Master File) is a document detailing the whole manufacturing process of Ritodrine active pharmaceutical ingredient (API) in detail. Different forms of Ritodrine DMFs exist exist since differing nations have different regulations, such as Ritodrine USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Ritodrine DMF submitted to regulatory agencies in the US is known as a USDMF. Ritodrine USDMF includes data on Ritodrine's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Ritodrine USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Ritodrine suppliers with USDMF on PharmaCompass.
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