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Diatrizoic acid
Cystografin, Gastrografin, Hypaque, Md, Sinografin, Urovist (diatrizoic acid) is a small molecule pharmaceutical. Diatrizoic acid was first approved as Cystografin on 1982-01-01.
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Commercial
Therapeutic Areas
No data
Trade Name
FDA
EMA
Cystografin (discontinued: Angiovist, Cardiografin, Hypaque, Md, Reno, Urovist, Urovist cysto)
Combinations
Gastrografin (generic drugs available since 1982-01-01, discontinued: Angiovist, Gastrovist, Hypaque, Md, Md-76r, Renocal, Renografin, Renovist, Sinografin)
Drug Products
FDA
EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
Diatrizoate meglumine
Tradename
Company
Number
Date
Products
CYSTOGRAFIN DILUTEBracco DiagnosticsN-010040 RX1982-11-09
1 products, RLD
CYSTOGRAFINBracco DiagnosticsN-010040 RX1982-01-01
1 products, RLD
Show 7 discontinued
Diatrizoate meglumine
+
Diatrizoate sodium
Tradename
Company
Number
Date
Products
GASTROGRAFINBracco DiagnosticsN-011245 RX1982-01-01
1 products, RLD, RS
Show 7 discontinued
Diatrizoate meglumine
+
Iodipamide meglumine
Tradename
Company
Number
Date
Products
SINOGRAFINBracco DiagnosticsN-011324 DISCN1982-01-01
1 products, RLD
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Diatrizoate sodium
Tradename
Company
Number
Date
Products
HYPAQUEGE HealthcareN-009561 DISCN1982-01-01
1 products
HYPAQUE SODIUM 20%GE HealthcareN-009561 DISCN1982-01-01
1 products
HYPAQUEGE HealthcareN-009561 DISCN1982-01-01
1 products
HYPAQUEGE HealthcareN-011386 DISCN1982-01-01
2 products
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Labels
FDA
EMA
Brand Name
Status
Last Update
cystografinNew Drug Application2018-04-15
gastrografinNew Drug Application2021-10-04
Indications
FDA
EMA
No data
Agency Specific
FDA
EMA
No data
Patent Expiration
No data
ATC Codes
V: Various drug classes in atc
— V08: Contrast media
— V08A: X-ray contrast media, iodinated
— V08AA: Watersoluble, nephrotropic, high osmolar x-ray contrast media
— V08AA01: Diatrizoic acid
HCPCS
No data
Clinical
Clinical Trials
16 clinical trials
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Indications Phases 4
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Congenital abnormalitiesD000013EFO_0003915Q89.9———1—1
GastroschisisD020139EFO_1000949Q79.3———1—1
Meconium ileusD000074270P76.0———1—1
Indications Phases 3
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
InfertilityD007246EFO_0000545——1——1
Urethral strictureD014525HP_0012227N35——1——1
Indications Phases 2
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Fecal impactionD005244K56.41—1———1
Indications Phases 1
No data
Indications Without Phase
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Intestinal obstructionD007415K56.60————11
Colorectal neoplasmsD015179————11
GallstonesD042882EFO_0004210————11
CholecystitisD002764HP_0001082K81————11
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameDIATRIZOIC ACID
INNsodium amidotrizoate
Description
Amidotrizoic acid is a member of the class of benzoic acids that is benzoic acid having iodo substituents at the 2-, 4- and 6-positions and acetamido substituents at the 3- and 5-positions. It is used, mainly as its N-methylglucamine and sodium salts, as an X-ray contrast medium in gastrointestinal studies, angiography, and urography. It has a role as a radioopaque medium, an environmental contaminant and a xenobiotic. It is an organoiodine compound, a member of benzoic acids and a member of acetamides. It is a conjugate acid of an amidotrizoic acid anion.
Classification
Small molecule
Drug class—
Image (chem structure or protein)
Structure (InChI/SMILES or Protein Sequence)
CC(=O)Nc1c(I)c(NC(C)=O)c(I)c(C(=O)O)c1I
Identifiers
PDB—
CAS-ID117-96-4
RxCUI1546223
ChEMBL IDCHEMBL1201220
ChEBI ID53691
PubChem CID2140
DrugBankDB00271
UNII IDV5403H8VG7 (ChemIDplus, GSRS)
Target
Agency Approved
No data
Alternate
No data
Variants
Clinical Variant
No data
Financial
No data
Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 29,446 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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261 adverse events reported
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