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01 2RITODRINE HCL
02 1YUTOPAR (RITODRINE HCL) TABLETS & INJECTION FORMS,OLST,HOLLAND
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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
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
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PharmaCompass offers a list of Ritodrine 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 Ritodrine manufacturer or Ritodrine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ritodrine manufacturer or Ritodrine supplier.
PharmaCompass also assists you with knowing the Ritodrine API Price utilized in the formulation of products. Ritodrine API Price is not always fixed or binding as the Ritodrine Price is obtained through a variety of data sources. The Ritodrine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A YUTOPAR (RITODRINE HCL) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of YUTOPAR (RITODRINE HCL), including repackagers and relabelers. The FDA regulates YUTOPAR (RITODRINE HCL) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. YUTOPAR (RITODRINE HCL) 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 YUTOPAR (RITODRINE HCL) manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A YUTOPAR (RITODRINE HCL) supplier is an individual or a company that provides YUTOPAR (RITODRINE HCL) active pharmaceutical ingredient (API) or YUTOPAR (RITODRINE HCL) finished formulations upon request. The YUTOPAR (RITODRINE HCL) suppliers may include YUTOPAR (RITODRINE HCL) API manufacturers, exporters, distributors and traders.
click here to find a list of YUTOPAR (RITODRINE HCL) suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A YUTOPAR (RITODRINE HCL) DMF (Drug Master File) is a document detailing the whole manufacturing process of YUTOPAR (RITODRINE HCL) active pharmaceutical ingredient (API) in detail. Different forms of YUTOPAR (RITODRINE HCL) DMFs exist exist since differing nations have different regulations, such as YUTOPAR (RITODRINE HCL) USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A YUTOPAR (RITODRINE HCL) DMF submitted to regulatory agencies in the US is known as a USDMF. YUTOPAR (RITODRINE HCL) USDMF includes data on YUTOPAR (RITODRINE HCL)'s chemical properties, information on the facilities and procedures used, and details about packaging and storage. The YUTOPAR (RITODRINE HCL) USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of YUTOPAR (RITODRINE HCL) suppliers with USDMF on PharmaCompass.