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AboutPricing
Drug ReportsMeglumine
Meglumine
Dibasic, Monobasic, Monohydrate, Phosphate (meglumine) is a small molecule pharmaceutical. Meglumine was first approved as Sodium phosphates in plastic container on 1983-05-10. It is used to treat aids-related opportunistic infections, cutaneous leishmaniasis, and visceral leishmaniasis in the USA.
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Commercial
Therapeutic Areas
Therapeutic Area
MeSH
infectionsD007239
skin and connective tissue diseasesD017437
immune system diseasesD007154
Trade Name
FDA
EMA
No data
Drug Products
FDA
EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
Calcium
+
Meglumine
+
Metrizoic acid
Tradename
Company
Number
Date
Products
ISOPAQUE 280GE HealthcareN-017506 DISCN1982-01-01
1 products
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FDA
EMA
Brand Name
Status
Last Update
baxdelaNew Drug Application2021-07-02
clariscanANDA2025-05-19
conrayNew Drug Application2023-05-11
cysto-conrayNew Drug Application2010-07-08
cysto-conray iiNew Drug Application2020-12-31
cystografinNew Drug Application2018-04-15
cystografin diluteNew Drug Application2018-10-02
diatrizoate meglumine and diatrizoate sodiumANDA2025-02-19
dotaremNew Drug Application2025-03-14
gadoterate meglumineANDA2025-04-16
Show 7 more
Agency Specific
FDA
EMA
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Patent Expiration
Patent
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FDA Information
Sodium Phosphate, Dibasic, Anhydrous / Sodium Phosphate, Monobasic, Monohydrate, Osmoprep, Salix Pharms
76870752028-06-22DS, DP
ATC Codes
P: Antiparasitic products, insecticides and repellents
P01: Antiprotozoals
P01C: Agents against leishmaniasis and trypanosomiasis
P01CB: Antimony compounds for treatment of leishmaniasis and trypanosomiasis
P01CB01: Meglumine antimonate
HCPCS
Code
Description
A9575
Injection, gadoterate meglumine, 0.1 ml
A9577
Injection, gadobenate dimeglumine (multihance), per ml
A9578
Injection, gadobenate dimeglumine (multihance multipack), per ml
Clinical
Clinical Trials
119 clinical trials
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Indications Phases 4
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
LeishmaniasisD007896EFO_0005044B55316164335
Cutaneous leishmaniasisD016773B55.1314142330
Healthy volunteers/patients11112
Ischemic strokeD00008324243228
StrokeD020521EFO_0000712I63.943127
IschemiaD007511EFO_000055643127
Cerebral infarctionD002544I6332126
AmyloidosisD000686EFO_1001875E851315
PolyneuropathiesD011115EFO_0009562A69.22134
Amyloid neuropathiesD017772134
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Indications Phases 1
Indications Without Phase
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
NeoplasmsD009369C8022
GliomaD005910EFO_000052022
Takotsubo cardiomyopathyD054549EFO_1002000I51.8111
Male breast neoplasmsD01856711
Autoimmune diseasesD001327EFO_0000540M30-M3611
Multiple sclerosisD009103EFO_0003885G3511
GlioblastomaD005909EFO_000051511
MedulloblastomaD00852711
GliosarcomaD01831611
Solitary fibrous tumorsD05436411
Show 39 more
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameMeglumine
INNmeglumine
Description
N-methylglucamine is a hexosamine that is D-glucitol in which the hydroxy group at position 1 is substituted by the nitrogen of a methylamino group. A crystalline base, it is used in preparing salts of certain acids for use as diagnostic radiopaque media, while its antimonate is used as an antiprotozoal in the treatment of leishmaniasis. It is a hexosamine and a secondary amino compound.
Classification
Small molecule
Drug class
Image (chem structure or protein)Loading
Structure (InChI/SMILES or Protein Sequence)
CNC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO
Identifiers
PDB
CAS-ID6284-40-8
RxCUI
ChEMBL IDCHEMBL1200570
ChEBI ID59732
PubChem CID8567
DrugBank
UNII ID6HG8UB2MUY (ChemIDplus, GSRS)
Target
No data
Variants
No data
Financial
Revenue by drug
$
£
Baxdela Melinta Therapeutics /new/
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Estimated US medical usage
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Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 10,853 documents
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Safety
Black-box Warning
Black-box warning for: Baxdela, Clariscan, Conray, Cysto-conray, Cysto-conray ii, Dotarem, Gadoterate meglumine
Adverse Events
Top Adverse Reactions
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12,248 adverse events reported
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