GASTROGRAFIN

This brand name is authorized in United States. It is also authorized in Canada, Croatia, Cyprus, Finland, Hong Kong SAR China, Ireland, Japan, Malta, New Zealand, Poland, Singapore, Spain, UK.

Active ingredients

The drug GASTROGRAFIN contains a combination of these active pharmaceutical ingredients (APIs):

1
UNII V5403H8VG7 - DIATRIZOATE SODIUM
 
Read more about Diatrizoic acid
2
UNII 3X9MR4N98U - DIATRIZOATE MEGLUMINE
 
Read more about Meglumine

Medication package inserts

Below package inserts are available for further reading:

Document Type Information Source  
 GASTROGRAFIN Gastroenteral solution MPI, EU: SmPC Medicines & Healthcare Products Regulatory Agency (GB)

Medicine classification

This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:

ATC Group Classification
P01CB01 Meglumine antimonate P Antiparasitic products, insecticides and repellents → P01 Antiprotozoals → P01C Agents against leishmaniasis and trypanosomiasis → P01CB Antimony compounds
Discover more medicines within P01CB01
V08AA01 Diatrizoic acid V Various → V08 Contrast media → V08A X-ray contrast media, iodinated → V08AA Watersoluble, nephrotropic, high osmolar X-ray contrast media
Discover more medicines within V08AA01

Authorization and marketing

This drug has been assigned below unique identifiers within the countries it is being marketed:

Country Identification scheme Identifier(s)
CA Health Products and Food Branch 02228564
ES Centro de información online de medicamentos de la AEMPS 36270
FI Lääkealan turvallisuus- ja kehittämiskeskus 027102
GB Medicines & Healthcare Products Regulatory Agency 97577
HK Department of Health Drug Office 46076
HR Agencija za lijekove i medicinske proizvode HR-H-901124749
JP 医薬品医療機器総合機構 7211001X1030
MT Medicines Authority AA565/52601, MA1354/00201
NZ Medicines and Medical Devices Safety Authority 2521
PL Rejestru Produktów Leczniczych 100025994, 100293631
SG Health Sciences Authority 05846P
US FDA, National Drug Code 0270-0445

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