01 Sanofi (1)
02 3D IMAGING DRUG DESIGN AND DEVELOPMENT LLC (1)
03 Deepwater Chemicals (1)
04 IBA MOLECULAR EASTERN ISOTOPES INC (1)
05 ISO TEX DIAGNOSTICS INC (1)
06 Lonza Biologics Inc (1)
07 MDS NORDION (1)
08 NTP Radioisotopes Soc Ltd (2)
09 PerkinElmer (2)
10 Blank (1)
01 BIOPAL VRO-20 (1)
02 FISSION IODINE-131 (1)
03 FISSION IODINE-131 (PRODUCED FROM LOW ENRICHED URANIUM(LEU) NORMAL PRODUCT (1)
04 IODINE (USP IODINE) (1)
05 IODINE 125 PRODUCED IN KANATA ISOTOPE PROCESSING FACIL (AECL-KIPE) (1)
06 IODINE I-125 (1)
07 IODINE-123 (D FORMERLY HELD BY UNION CARBIDE CORP) (1)
08 IODINE-124 (1)
09 IODINE-125 (1)
10 IODINE-131-PRODUCED IN NORTH BILLERICA, MA. (1)
11 TOSITUMOMAB [MURINE MONOCLONAL ANTIBODY (B1) AGAINST B LYMPHOCYTES (CD20)] (1)
12 [I-124]CLR1404 INJECTION (1)
01 Belgium (1)
02 Canada (1)
03 France (1)
04 South Africa (2)
05 U.S.A (6)
06 Blank (1)
01 Active (3)
02 Inactive (9)
01 Complete (1)
02 Blank (11)
64
PharmaCompass offers a list of Iodine 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 Iodine manufacturer or Iodine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Iodine manufacturer or Iodine supplier.
PharmaCompass also assists you with knowing the Iodine API Price utilized in the formulation of products. Iodine API Price is not always fixed or binding as the Iodine Price is obtained through a variety of data sources. The Iodine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 03551_FLUKA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 03551_FLUKA, including repackagers and relabelers. The FDA regulates 03551_FLUKA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 03551_FLUKA 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 03551_FLUKA manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A 03551_FLUKA supplier is an individual or a company that provides 03551_FLUKA active pharmaceutical ingredient (API) or 03551_FLUKA finished formulations upon request. The 03551_FLUKA suppliers may include 03551_FLUKA API manufacturers, exporters, distributors and traders.
click here to find a list of 03551_FLUKA suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A 03551_FLUKA DMF (Drug Master File) is a document detailing the whole manufacturing process of 03551_FLUKA active pharmaceutical ingredient (API) in detail. Different forms of 03551_FLUKA DMFs exist exist since differing nations have different regulations, such as 03551_FLUKA USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A 03551_FLUKA DMF submitted to regulatory agencies in the US is known as a USDMF. 03551_FLUKA USDMF includes data on 03551_FLUKA's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The 03551_FLUKA USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of 03551_FLUKA suppliers with USDMF on PharmaCompass.
We have 9 companies offering 03551_FLUKA
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