01 DOTTIKON EXCLUSIVE SYNTHESIS AG (1)
02 Dipharma (1)
03 Industriale Chimica s.r.l. (1)
04 Kremers Urban Pharmaceuticals Inc. (1)
05 Lunan Pharmaceutical (1)
06 Lusochimica SPA (1)
07 Mallinckrodt Pharmaceuticals (1)
08 Nitto Denko Avecia (2)
09 Stuart Therapeutics (1)
10 Blank (5)
01 DILUTED ISOSORBIDE DINITRATE (1)
02 DILUTED ISOSORBIDE DINITRATE USP (1)
03 ISORBIDE DINITRATE C.R. CAPS 80MG (1)
04 ISOSORBIDE DINITRATE (3)
05 ISOSORBIDE DINITRATE (ISDN) (1)
06 ISOSORBIDE DINITRATE DILUTED (1)
07 ISOSORBIDE DINITRATE INJECTION (50ML AND 100ML) (1)
08 ISOSORBIDE DINITRATE TIMED RELEASE PELLETS (1)
09 ISOSORBIDE DINITRATE TRANSDERMAL SUSPENSION (1)
10 ISOSORBIDE DINITRATE, DILUTED (1)
11 SDM 50 (STABILIZED 50/50 ISOSORBIDE DINITRATE-LACTOSE MIXTURE) (1)
12 SDM-25 (25/75 ISOSORBIDE DINITRATE-MANNITOL MIXTURE) (1)
13 SDM-40 (25% ISOSORBIDE DINITRATE IN LACTOSE) (1)
01 China (1)
02 Ireland (1)
03 Italy (3)
04 Switzerland (1)
05 U.S.A (4)
06 Blank (5)
01 Active (4)
02 Inactive (11)
01 Complete (2)
02 Blank (13)
33
PharmaCompass offers a list of Isosorbide Dinitrate 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 Isosorbide Dinitrate manufacturer or Isosorbide Dinitrate supplier for your needs.
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PharmaCompass also assists you with knowing the Isosorbide Dinitrate API Price utilized in the formulation of products. Isosorbide Dinitrate API Price is not always fixed or binding as the Isosorbide Dinitrate Price is obtained through a variety of data sources. The Isosorbide Dinitrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Prestwick3_000714 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Prestwick3_000714, including repackagers and relabelers. The FDA regulates Prestwick3_000714 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Prestwick3_000714 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 Prestwick3_000714 supplier is an individual or a company that provides Prestwick3_000714 active pharmaceutical ingredient (API) or Prestwick3_000714 finished formulations upon request. The Prestwick3_000714 suppliers may include Prestwick3_000714 API manufacturers, exporters, distributors and traders.
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A Prestwick3_000714 DMF (Drug Master File) is a document detailing the whole manufacturing process of Prestwick3_000714 active pharmaceutical ingredient (API) in detail. Different forms of Prestwick3_000714 DMFs exist exist since differing nations have different regulations, such as Prestwick3_000714 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Prestwick3_000714 DMF submitted to regulatory agencies in the US is known as a USDMF. Prestwick3_000714 USDMF includes data on Prestwick3_000714's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Prestwick3_000714 USDMF is kept confidential to protect the manufacturer’s intellectual property.
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We have 9 companies offering Prestwick3_000714
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