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Search results for nonoxynol root_codes_@count in @count (approximate match)
Status:
US Approved Rx
(2019)
Source:
ANDA210016
(2019)
Source URL:
First approved in 1988
Source:
MAGNEVIST by BAYER HLTHCARE
Source URL:
Class (Stereo):
CHEMICAL (ACHIRAL)
Conditions:
DOTAREM (Gadoterate Meglumine ) is a gadolinium-based contrast agent indicated for intravenous use with magnetic resonance imaging (MRI) in brain (intracranial), spine and associatedtissues in adult and pediatric patients (2 years of age and older) to detect and visualize areas with disruption of the blood brain barrier (BBB) and/or abnormal vascularity. Gadoterate Meglumine is a gadolinium chelate paramagnetic contrast agent. When placed in a magnetic field, gadoterate meglumine produces a large magnetic moment and so a large local magnetic field, which can enhance the relaxation rate of nearby protons; as a result, the signal intensity of tissue images observed with magnetic resonance imaging (MRI) may be enhanced. Because this agent is preferentially taken up by normal functioning hepatocytes, normal hepatic tissue is enhanced with MRI while tumor tissue is unenhanced. In addition, because gadobenate dimeglumine is excreted in the bile, it may be used to visualize the biliary system using MRI.
Status:
US Approved Rx
(2015)
Source:
ANDA204517
(2015)
Source URL:
First approved in 1972
Source:
FLUORINE F-18 by GE HEALTHCARE
Source URL:
Class (Stereo):
CHEMICAL (ACHIRAL)
Conditions:
FLUORIDE ION F-18 (as sodium fluoride F-18) is a radioactive diagnostic agent for positron emission tomography (PET) indicated for imaging of bone to define areas of altered osteogenic activity. FLUORIDE ION F-18 normally accumulates in the skeleton in an even fashion, with greater deposition in the axial skeleton (e.g. vertebrae and pelvis) than in the appendicular skeleton and greater deposition in the bones around joints than in the shafts of long bones. Increased FLUORIDE ION F-18 deposition in the bone can occur in areas of increased osteogenic activity during growth, infection, malignancy (primary or metastatic) following trauma, or inflammation of the bone.
Status:
US Approved Rx
(1972)
Source:
NDA016968
(1972)
Source URL:
First approved in 1972
Source:
NDA016968
Source URL:
Class (Stereo):
CHEMICAL (ACHIRAL)
Conditions:
Carbachol is a potent cholinergic (parasympathomimetic) agent which produces constriction of the iris and ciliary body resulting in reduction in intraocular pressure.
Status:
US Approved Rx
(1962)
Source:
NDA050356
(1962)
Source URL:
First approved in 1953
Source:
BIOMYDRIN W/HC THONZONIUM BROMIDE by BW
Source URL:
Class (Stereo):
CHEMICAL (ACHIRAL)
Targets:
Conditions:
Thonzonium Bromide is a cationic surface-active compound. As an additive to pharmacologic formulations, thonzonium bromide causes dispersion and penetration of cellular debris and exudate, thereby promoting tissue contact of the administered medication. Thonzonium
bromide is a component of FDA-approved Coly-Mycin S Otic, used for treating infections of the ear caused by certain bacteria. It has being shown that Thonzonium bromide inhibits RANKL-induced osteoclast formation and bone resorption in vitro and prevents LPS-induced bone loss in vivo, suggesting that Thonzonium bromide might be a useful alternative therapy in preventing or treating osteolytic diseases..
Status:
US Approved OTC
Source:
21 CFR 331.11(g)(3) antacid:magnesium-containing magnesium aluminosilicate
Source URL:
First approved in 1955
Source:
ANDA210543
Source URL:
Class (Stereo):
CHEMICAL (ACHIRAL)
Conditions:
Magnesium aluminosilicate is an antacid, it is used in combination with magnesium hydroxide to relieve heartburn.
Status:
US Animal Drug
Source:
21 CFR 520.1802a PART 520-ORAL DOSAGE FORM NEW ANIMAL DRUGS piperazine-carbon disulfide complex
Source URL:
Class (Stereo):
CHEMICAL (ACHIRAL)
Picadex is a dithiocarbamate derivative of piperazine. It was used in veterinary as an antihelmintic drug. It was shown to be effective in the treatment of Oesophagostamum infection in pigs.
Status:
Investigational
Source:
Am J Dent. Feb 2002;15(1):8-10.: Phase 2 Human clinical trial Completed N/A
Source URL:
Class (Stereo):
CHEMICAL (MIXED)
Status:
Investigational
Source:
NCT02649790: Phase 1/Phase 2 Interventional Completed Relapsed/Refractory Multiple Myeloma (RRMM)
(2016)
Source URL:
Class (Stereo):
CHEMICAL (ACHIRAL)
Targets:
Eltanexor (KPT-8602) is an investigational second-generation Selective Inhibitor of Nuclear Export (SINE) compound that is designed to selectively block the nuclear export protein XPO1. Most of the key tumor suppressor proteins (TSPs), are cargos of XPO1 and inhibition of XPO1 by eltanexor is believed to sequester TSPs in the nucleus where they can carry out their normal functions. Karyopharm Therapeutics is developing eltanexor for the treatment of relapsed/refractory cancers.
Status:
Investigational
Source:
NCT04533581: Phase 2 Interventional Active, not recruiting Indolent B-cell Non-Hodgkin's Lymphoma
(2020)
Source URL:
Class (Stereo):
CHEMICAL (ACHIRAL)
Status:
Investigational
Source:
NCT04440007: Phase 2 Interventional Completed Covid-19
(2020)
Source URL:
Class (Stereo):
CHEMICAL (ACHIRAL)