Olpha, a JSC AB City subsidiary, is a leading Baltic firm with 50 years of experience in medicines & chemical pharmaceuticals.
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01 1Olpha
02 1Cilag AG
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01 2RIMANTADINE HYDROCHLORIDE
02 1RIMANTADINE HYDROCHLORIDE, NON-STERILE BULK DRUG SUBSTANCE CW-100
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01 1Latvia
02 1Switzerland
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01 1Active
02 2Inactive
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01 1Complete
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Olpha, a JSC AB City subsidiary, is a leading Baltic firm with 50 years of experience in medicines & chemical pharmaceuticals.
GDUFA
DMF Review : Complete
Rev. Date : 2014-06-17
Pay. Date : 2012-11-27
DMF Number : 15210
Submission : 2000-12-21
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 10233
Submission : 1993-05-05
Status : Inactive
Type : II
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 14936
Submission : 2000-06-22
Status : Inactive
Type : II
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PharmaCompass offers a list of Rimantadine Hydrochloride 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 Rimantadine Hydrochloride manufacturer or Rimantadine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Rimantadine Hydrochloride manufacturer or Rimantadine Hydrochloride supplier.
PharmaCompass also assists you with knowing the Rimantadine Hydrochloride API Price utilized in the formulation of products. Rimantadine Hydrochloride API Price is not always fixed or binding as the Rimantadine Hydrochloride Price is obtained through a variety of data sources. The Rimantadine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Flumadine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Flumadine, including repackagers and relabelers. The FDA regulates Flumadine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Flumadine 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 Flumadine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Flumadine supplier is an individual or a company that provides Flumadine active pharmaceutical ingredient (API) or Flumadine finished formulations upon request. The Flumadine suppliers may include Flumadine API manufacturers, exporters, distributors and traders.
click here to find a list of Flumadine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Flumadine DMF (Drug Master File) is a document detailing the whole manufacturing process of Flumadine active pharmaceutical ingredient (API) in detail. Different forms of Flumadine DMFs exist exist since differing nations have different regulations, such as Flumadine USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Flumadine DMF submitted to regulatory agencies in the US is known as a USDMF. Flumadine USDMF includes data on Flumadine's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Flumadine USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Flumadine suppliers with USDMF on PharmaCompass.