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Displaying drugs 76 - 100 of 9336 in total

Efavirenz

Efavirenz (brand names Sustiva® and Stocrin®) is a non-nucleoside reverse transcriptase inhibitor (NNRTI) and is used as part of highly active antiretroviral therapy (HAART) for the treatment of a human immunodeficiency virus (HIV) type 1. For HIV infection that has not previously been treated, efavirenz and lamivudine in combination with...
Approved
Investigational
Matched Description: … Efavirenz is also used in combination with other antiretroviral agents as part of an expanded postexposure …

Danazol

A synthetic steroid with antigonadotropic and anti-estrogenic activities that acts as an anterior pituitary suppressant by inhibiting the pituitary output of gonadotropins. It possesses some androgenic properties. Danazol has been used in the treatment of endometriosis and some benign breast disorders.
Approved
Matched Description: … A synthetic steroid with antigonadotropic and anti-estrogenic activities that acts as an anterior pituitary …

Activated charcoal

Activated charcoal, or activated carbon, is an amorphous form of carbon prepared from incomplete combustion of carbonaceous organic matter. It is activated by an oxidizing gas flow at high temperature passed over its surface to make a fine network of pores, producing a material with large surface area and high...
Approved
Matched Description: … Activated charcoal, or activated carbon, is an amorphous form of carbon prepared from incomplete combustion ... It is activated by an oxidizing gas flow at high temperature passed over its surface to make a fine network …

Calcium levulinate

The relatively new calcium levulinate is produced from a direct reaction between L- or levulinic acid levulose and calcium hydroxide . The resultant calcium levulinate formulation, when used as a calcium supplement, possesses a high calcium content that is observed to be 14.8% higher than the content typically found in...
Approved
Experimental

Nogapendekin alfa

Nogapendekin alfa is a human IL-15N72D variant. It is one of the active ingredients in Anktiva, a combination product also containing inbakicept, where a single inbakicept is complexed with two nogapendekin alfa components. This combination product was approved by the FDA on April 22, 2024, for the treatment of BCG-unresponsive...
Approved
Investigational
Matched Description: … [L50592] This combination product was approved by the FDA on April 22, 2024, for the treatment of BCG-unresponsive …

Hydromorphone

Hydromorphone is a pure opioid, a semi-synthetic hydrogenated ketone derivative of morphine that has been available clinically since 1920. Structurally, hydromorphone derived from morphine in the modification of the hydroxyl group in the carbon 6 to a carbonyl and the absence of a double bond between the carbon 7 and...
Approved
Illicit
Matched Description: … hydrochloride was developed by Fresenius Kabi USA and FDA approved in 1984. ... Structurally, hydromorphone derived from [morphine] in the modification of the hydroxyl group in the ... [A176471] Even though hydromorphone does not present a 6-hydroxyl group, it is categorized under the …

Titanium dioxide

Titanium dioxide, also known as titanium(IV) oxide or titania, is the naturally occurring oxide of titanium. It is used as a pigment under the names titanium white, Pigment White 6 (PW6), or CI 77891. It is typically extracted from ilmenite, rutile and anatase.
Approved
Matched Mixtures name: … Seoyoon Hanbang Ja An Cover BB Cream …
Matched Products: … An Adc Whitening Bb ... An Adc Sp Intensive Bb …

Amoxicillin

Amoxicillin, or BRL-2333, is a penicillin G derivative first described in the literature in 1972. Amoxicillin has similar activity to penicillin and ampicillin, but leads to higher serum concentrations than ampicillin. Amoxicillin was granted FDA approval on 18 January 1974.
Approved
Vet approved
Matched Mixtures name: … Truemed Group LLC ... AMOXICILLINA E ACIDO CLAVULANICO TEVA GROUP ... AMOXICILLINA E ACIDO CLAVULANICO TEVA GROUP …

Iobenguane sulfate I-123

Iobenguane sulfate I-123 is a radiopharmaceutical used in gamma-scintigraphy of adrenergically inervated tissues [FDA Label].
Approved
Investigational
Matched Categories: … Radioactive Diagnostic Agent …

Parachlorophenol

P-chlorophenol is a white crystals with a strong phenol odor. Slightly soluble to soluble in water, depending on the isomer, and denser than water. Noncombustible.
Approved

Ifosfamide

Ifosfamide is a chemotherapeutic agent chemically related to the nitrogen mustards and a synthetic analog of cyclophosphamide. It is active as an alkylating agent and an immunosuppressive agent.
Approved
Matched Description: … It is active as an alkylating agent and an immunosuppressive agent. ... Ifosfamide is a chemotherapeutic agent chemically related to the nitrogen mustards and a synthetic analog …

Technetium Tc-99m pyrophosphate

A radionuclide imaging agent used primarily in scintigraphy or tomography of the heart to evaluate the extent of the necrotic myocardial process. It has also been used in noninvasive tests for the distribution of organ involvement in different types of amyloidosis and for the evaluation of muscle necrosis in the...
Approved
Matched Description: … A radionuclide imaging agent used primarily in scintigraphy or tomography of the heart to evaluate the …
Matched Categories: … Radioactive Diagnostic Agent …

Idecabtagene vicleucel

Multiple myeloma is a cancer where plasma cells rapidly divide out of control. These cancerous cells generally express the B-cell maturation antigen, while it is rarely expressed on non-cancerous cells. Multiple myeloma is typically treated with an immunomodulatory agent like lenalidomide, a proteasome inhibitor like bortezomib, or an anti-CD38 monoclonal...
Approved
Matched Description: … [A232563] Multiple myeloma is typically treated with an immunomodulatory agent like [lenalidomide],[A232593 ... ] a proteasome inhibitor like [bortezomib], or an anti-CD38 monoclonal antibody like [isatuximab]. ... [A232558] The chimeric antigen receptor of idecabtagene vicleucel includes an anti-B-cell maturation …

Mangafodipir

Mangafodipir is a contrast agent used as a diagnostic tool administered intravenously to enhance contrast in magnetic resonance imaging (MRI) of the liver and pancreas. This drug is made up of paramagnetic manganese (II) ions combined with the chelating agent fodipir (dipyridoxyl diphosphate, DPDP). Manganese absorption into the tissues that...
Approved
Investigational
Withdrawn
Matched Description: … The contrast agent is present as mangafodipir trisodium marketed under the name Teslascan. ... Mangafodipir is a contrast agent used as a diagnostic tool administered intravenously to enhance contrast ... This drug is made up of paramagnetic manganese (II) ions combined with the chelating agent _fodipir_ …
Matched Categories: … Paramagnetic Contrast Agent …

Gadopiclenol

Gadopiclenol is a gadolinium-based contrast agent (GBCA) based on a pyclen macrocyclic structure. It is indicated for use with magnetic resonance imaging (MRI) to detect and visualize lesions with abnormal vascularity in the central nervous system and the body. In 2006, the use of GBCAs was associated with the development...
Approved
Matched Description: … Gadopiclenol is a gadolinium-based contrast agent (GBCA) based on a pyclen macrocyclic structure. ... [A254002,A254017] In September 2022, the use of gadopiclenol was approved by the FDA. …
Matched Categories: … Paramagnetic Contrast Agent ... Gadolinium-based Contrast Agent …

Gluconolactone

Gluconolactone is a naturally-occurring food additive used as a sequestrant, an acidifier, or a curing, pickling, or leavening agent. It is a cyclic ester of D-gluconic acid. Pure gluconolactone is a white odorless crystalline powder.
Approved
Experimental
Matched Description: … , pickling, or leavening agent. ... Gluconolactone is a naturally-occurring food additive used as a sequestrant, an acidifier, or a curing …
Matched Categories: … Calculi Dissolution Agent …

Dasiglucagon

Dasiglucagon is a glucagon analog that acts to increase blood sugar levels. It consists of 29 amino acids similar to endogenous glucagon; however, it contains seven substituted amino acids for improved physical and chemical stability in its drug formulation. In March 2021, the FDA approved dasiglucagon to treat severe hypoglycemia...
Approved
Investigational
Matched Description: … [L39190] Severe hypoglycemia is an acute, life-threatening medical condition resulting from a profound ... [L39195] In March 2021, the FDA approved dasiglucagon to treat severe hypoglycemia in patients six years ... [L39195] The approval of dasiglucagon marks the first glucagon analog approved for severe hypoglycemia …
Matched Categories: … Antihypoglycemic Agent …

Belantamab mafodotin

Belantamab mafodotin, or GSK2857916, is an afucosylated monoclonal antibody that targets B cell maturation antigen conjugated to the microtubule disrupter monomethyl auristatin-F (MMAF). Belantamab mafodotin was granted FDA accelerated approval on 5 August 2020 for the treatment of multiple myeloma; however, its manufacturer began the process for withdrawal of the...
Approved
Matched Description: … Belantamab mafodotin, or GSK2857916, is an afucosylated monoclonal antibody that targets B cell maturation …
Matched Categories: … Tubulin Inhibiting Agent …

Voxilaprevir

Voxilaprevir is a Direct-Acting Antiviral (DAA) medication used as part of combination therapy to treat chronic Hepatitis C, an infectious liver disease caused by infection with Hepatitis C Virus (HCV). HCV is a single-stranded RNA virus that is categorized into nine distinct genotypes, with genotype 1 being the most common...
Approved
Investigational
Matched Description: … an HCV regimen containing sofosbuvir without an NS5A inhibitor [L935]. ... Vosevi is approved for the treatment of adult patients with chronic HCV infection with genotype 1, 2, ... Prior to Vosevi, there were no approved retreatment options for patients who have previously received …

Tozinameran

The Pfizer-BioNTech COVID-19 vaccine (also known as BNT162b2, Tozinameran, and Comirnaty), is one of four advanced mRNA-based vaccines developed through "Project Lightspeed," a joint program between Pfizer and BioNTech.[L15002,L15007,L36025] Comirnaty is a nucleoside modified mRNA (modRNA) vaccine encoding an optimized full-length version of the severe acute respiratory syndrome coronavirus 2...
Approved
Investigational
Matched Description: … [L15002,L15007,L36025] Comirnaty is a nucleoside modified mRNA (modRNA) vaccine encoding an optimized ... Comirnaty is also approved for use as a fourth booster shot in adults 50 years of age and older. ... [L26966,L26976] In November 2021, Health Canada [L39115] and the EMA [L39272] approved the vaccine to …

Technetium Tc-99m tilmanocept

Technetium Tc-99m tilmanocept is a radiopharmaceutical diagnostic imaging agent approved by the U.S. Food and Drug Administration (FDA) for the imaging of lymph nodes with or without scintigraphic imaging. It is a macromolecule consisting of multiple units of diethylenetriaminepentaacetic acid (DTPA) and mannose, each covalently attached to a 10 kDa...
Approved
Investigational
Matched Description: … Technetium Tc-99m tilmanocept is a radiopharmaceutical diagnostic imaging agent approved by the U.S. ... DTPA serves as a chelating agent for technetium Tc 99m to bind [FDA Label]. …
Matched Categories: … Radioactive Diagnostic Agent …

Vestronidase alfa

Vestronidase alfa, or vestronidase alfa-vjbk, is a recombinant human lysosomal beta glucuronidase that is a purified enzyme produced by recombinant DNA technology in a Chinese hamster ovary cell line. The enzyme is a homotetramer consisted of 4 monomers with 629 amino acids, and holds the same amino acid sequence as...
Approved
Investigational
Matched Description: … Vestronidase alfa was FDA-approved on November 17th, 2017 under the trade name Mepsevii as an intravenous ... Vestronidase alfa is an enzyme replacement therapy for the treatment of mucopolysaccharidosis type VII ... (MPS VII), also known as Sly syndrome, which is an inherited, rare genetic metabolic condition that …

Aluminum sesquichlorohydrate

Aluminum sesquichlorohydrate is an aluminum salt used as an antiperspirant agent, cosmetic astringent and deodorant agent. It works by physically blocking eccrine sweat gland ducts .
Approved
Matched Description: … Aluminum sesquichlorohydrate is an aluminum salt used as an antiperspirant agent, cosmetic astringent ... and deodorant agent. …

Ketamine

Ketamine is an NMDA receptor antagonist with a potent anesthetic effect. It was developed in 1963 as a replacement for phencyclidine (PCP) by Calvin Stevens at Parke Davis Laboratories. It started being used for veterinary purposes in Belgium and in 1964 was proven that compared to PCP, it produced minor...
Approved
Vet approved
Matched Description: … It was FDA approved in 1970, and from there, it has been used as an anesthetic for children or patients ... Ketamine is an NMDA receptor antagonist with a potent anesthetic effect. …

Besilesomab

Besilesomab is a mouse monoclonal antibody labelled with the radioactive isotope technetium-99m for determining the location of inflammation/infection in peripheral bone in adults with suspected osteomyelitis [FDA Label]. Utilised only as a diagnostic agent, besilesomab is currently approved by the EMEA for marketing and use in various European countries like...
Approved
Matched Description: … Utilised only as a diagnostic agent, besilesomab is currently approved by the EMEA for marketing and …
Displaying drugs 76 - 100 of 9336 in total