CYSTOGRAFIN ® Diatrizoate Meglumine Injection USP 30%

Manufacturer
BRACCO DIAGNOSTICS INC | PATHEON ITALIA SPA | Justesa Imagen, S.A.U
Effective date
2025-11-23
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
7
Source
full-release
Hydrated at
2026-05-31 21:47:56

Label at a glance#

ProductCystografin
Active ingredientdiatrizoate meglumine
Label structure11 sections

Dosage and administration

Preparation of the patient: Appropriate preparation is desirable for optimal results. A laxative the night before the examination and a low residue diet the day before the procedure are recommended. Dosage: The dose for retrograde use in cystography and voiding cystourethrography ranges from 25 to 300 mL depending on the age of the patient and the degree of bladder irritability; amounts greater than 300 mL may be ...

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

For retrograde cystourethrography
Not intended for intravascular injection

DESCRIPTION

DESCRIPTION SECTION

Cystografin is a radiopaque contrast agent supplied as a sterile, clear, colorless to pale yellow, mobile or slightly viscous solution. Each mL provides 300 mg diatrizoate meglumine with 0.4 mg edetate disodium as a sequestering agent. Each mL of solution also contains approximately 141 mg organically bound iodine. At the time of manufacture, the air in the container is replaced by nitrogen. The preparation should be protected from strong light.

INDICATION

INDICATIONS & USAGE SECTION

Cystografin is indicated for retrograde cystourethrography.

CONTRAINDICATIONS

CONTRAINDICATIONS SECTION

This preparation is contraindicated in patients with a hypersensitivity to salts of diatrizoic acid.

WARNINGS

WARNINGS SECTION

Severe sensitivity reactions are more likely to occur in patients with a personal or family history of bronchial asthma, significant allergies, or previous reactions to contrast agents.

A history of sensitivity to iodine per se or to other contrast agents is not an absolute contraindication to the use of diatrizoate meglumine, but calls for extreme caution in administration.

PRECAUTIONS

PRECAUTIONS SECTION

Safe and effective use of this preparation depends upon proper dosage, correct technique, adequate precautions, and readiness for emergencies.

Retrograde cystourethrography should be performed with caution in patients with a known active infectious process of the urinary tract.

Sterile technique should be employed in administration. During administration, care should be taken to avoid excessive pressure, rapid or acute distention of the bladder, and trauma.

Contrast agents may interfere with some chemical determinations made on urine specimens; therefore, urine should be collected before administration of the contrast medium or two or more days afterwards.

Pregnancy—Teratogenic Effects:

TERATOGENIC EFFECTS SECTION

Animal reproduction studies have not been conducted with diatrizoate meglumine injection. It is also not known whether diatrizoate meglumine injection can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. Cystografin should be administered to a pregnant woman only if clearly needed.

ADVERSE REACTIONS

ADVERSE REACTIONS SECTION

Retrograde genitourinary procedures may cause such complications as hematuria, perforation of the urethra or bladder, introduction of infection into the genitourinary tract, and oliguria or anuria.

If intravasation of this drug occurs, the reactions which may be associated with intravenous administration may possibly be encountered. Hypersensitivity or anaphylactoid reactions may occur. Severe reactions may be manifested by edema of the face and glottis, respiratory distress, convulsions or shock; such reactions may prove fatal unless promptly controlled by such emergency measures as maintenance of a clear airway and immediate use of oxygen and resuscitative drugs.

Endocrine: Thyroid function tests indicative of hypothyroidism or transient thyroid suppression have been uncommonly reported following iodinated contrast media administration to adult and pediatric patients, including infants. Some patients were treated for hypothyroidism.

DOSAGE AND ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

SPL UNCLASSIFIED SECTION

Preparation of the patient: Appropriate preparation is desirable for optimal results. A laxative the night before the examination and a low residue diet the day before the procedure are recommended.

SPL UNCLASSIFIED SECTION

Dosage: The dose for retrograde use in cystography and voiding cystourethrography ranges from 25 to 300 mL depending on the age of the patient and the degree of bladder irritability; amounts greater than 300 mL may be used if the bladder capacity allows. Best results are obtained when the bladder is filled with the contrast agent. If desired, the preparation may be diluted with sterile water or sterile saline as indicated in the table below.

SPL UNCLASSIFIED SECTION

Administration: After sterile catheterization, the bladder should be filled to capacity with Cystografin using a suitable sterile administration set. Care should be taken to avoid using excessive pressure. The presence of bladder discomfort or reflux and/or spontaneous voiding usually indicates that the bladder is full.

SPL UNCLASSIFIED SECTION

Radiography: The commonly employed radiographic techniques should be used. A scout film is recommended before the contrast agent is administered.

Dilution Table
USE DILUTED SOLUTIONS IMMEDIATELY
100 mL Bottle 
Sterile Water or Sterile Saline Added % Diatrizoate Meglumine w/v% Organically Bound Iodine w/v Total Volume
0 mL 30.0 14.1 100 mL
25 mL 24.0 11.3 125 mL
50 mL 20.09.4 150 mL
67 mL 18.0 8.5 167 mL
300 mL Bottle 
Sterile Water or Sterile Saline Added 
0 mL 30.0 14.1 300 mL
50 mL 25.7 12.1 350 mL

HOW SUPPLIED

HOW SUPPLIED SECTION

Cystografin (Diatrizoate Meglumine Injection USP 30%) is available in 200 mL and 400 mL bottles containing 100 mL and 300 mL of Cystografin respectively with sufficient capacity for dilution up to 167 mL and 350 mL respectively.

Storage

STORAGE AND HANDLING SECTION

Store at 20-25°C (68-77°F) [See USP]. Protect from light.

Also Available

SPL UNCLASSIFIED SECTION

Cystografin Dilute (Diatrizoate Meglumine Injection USP 18%) is also available, as a 300 mL fill in a 400 mL bottle.

SPL UNCLASSIFIED SECTION

Revised June 2024 

Rx only

Manufactured for
Bracco Diagnostics Inc.
Princeton, NJ 08540

by Patheon Italia S.p.A.
03013 Ferentino (Italy)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Cystografin 100 mL Label
NDC 0270-0149-60

Cystografin 100 mL Label
Cystografin 100 mL Label

Cystografin 1 Box 10 Bottles — 300 mL each
NDC 0270-0149-57

Cystografin 1 Box 10 Bottles — 300 mL
Cystografin 1 Box 10 Bottles — 300 mL

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
DIATRIZOIC ACID Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
a8f1679b-19b1-407c-9ee3-d33055bee6fcProduct name220250731

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0270-0149-57Cystografin10 in 1 PACKAGEINJECTION, SOLUTION107
0270-0149-57Cystografin300 mL in 1 BOTTLEINJECTION, SOLUTION3007
0270-0149-60Cystografin10 in 1 PACKAGEINJECTION, SOLUTION107
0270-0149-60Cystografin100 mL in 1 BOTTLEINJECTION, SOLUTION1007

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0270-0149-57ML - Milliliter0270-0149edfa8868-1b15-483d-890e-b15b2c83dd5412013-02-13
0270-0149-60ML - Milliliter0270-01497e901fa0-0046-48d2-af20-0a7abca18e1412013-02-13

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
diatrizoate meglumineACTIVE INGREDIENT3X9MR4N98U5
diatrizoic acidACTIVE MOIETY5UVC90J1LK5
edetate disodiumINACTIVE INGREDIENT7FLD91C86K5

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0270-01490270-0149-60, 0270-0149-57

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
diatrizoate meglumine3X9MR4N98UACTIB
edetate disodium7FLD91C86KIACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 3 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
edetate disodiumEDETATE DISODIUM7FLD91C86KINJECTION, SOLUTION / INTRAVENOUS7 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates
edetate disodiumEDETATE DISODIUM7FLD91C86KINJECTION, SOLUTION / INTRAVENOUS7 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates
edetate disodiumEDETATE DISODIUM7FLD91C86KINJECTION, SOLUTION / INTRAVENOUS7 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates

Orange Book application contexts#

All distinct exact application/product contexts derived from this label’s complete NDC list are paginated below.

Orange Book application contexts page 1 of 1 · 1 matching rows.

Source provenance: Browse the complete Orange Book source catalog · source snapshot 44.

Orange Book products#

Current product rows page 1 of 1 · 10 matching rows.

Application-product, Trade name, Ingredient table
Application-productTrade nameIngredientStrengthDosage form / routeTE codesRLD / RSApproval date
N010040-001RENOGRAFIN-76DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM66%;10%INJECTABLE / INJECTIONRLD, Approved before 1982
N010040-006RENOGRAFIN-60DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM52%;8%INJECTABLE / INJECTIONApproved before 1982
N010040-012RENO-DIPDIATRIZOATE MEGLUMINE30%INJECTABLE / INJECTIONApproved before 1982
N010040-016RENO-60DIATRIZOATE MEGLUMINE60%INJECTABLE / INJECTIONApproved before 1982
N010040-017DIATRIZOATE MEGLUMINEDIATRIZOATE MEGLUMINE76%INJECTABLE / INJECTIONApproved before 1982
N010040-018CYSTOGRAFINDIATRIZOATE MEGLUMINE30%SOLUTION / URETHRALRLD, Approved before 1982
N010040-019RENOVIST IIDIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM28.5%;29.1%INJECTABLE / INJECTIONApproved before 1982
N010040-020RENOVISTDIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM34.3%;35%INJECTABLE / INJECTIONApproved before 1982
N010040-021RENO-30DIATRIZOATE MEGLUMINE30%SOLUTION / URETERALApproved before 1982
N010040-022CYSTOGRAFIN DILUTEDIATRIZOATE MEGLUMINE18%SOLUTION / URETHRALRLD1982-11-09

Observed Orange Book product history#

Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.

Product history page 1 of 11 · 440 observed states.

Captured, Edition, Application-product table
CapturedEditionApplication-productTrade nameStrengthDosage form / routeProduct TE source textRLD / RSApproval dateSource SHA-256
2026-10-15 13:18:302026-09N010040-001RENOGRAFIN-7666%;10%INJECTABLE / INJECTIONRLD, Approved before 1982c2088c7a36db…
2026-10-15 13:18:302026-09N010040-006RENOGRAFIN-6052%;8%INJECTABLE / INJECTIONApproved before 1982c2088c7a36db…
2026-10-15 13:18:302026-09N010040-012RENO-DIP30%INJECTABLE / INJECTIONApproved before 1982c2088c7a36db…
2026-10-15 13:18:302026-09N010040-016RENO-6060%INJECTABLE / INJECTIONApproved before 1982c2088c7a36db…
2026-10-15 13:18:302026-09N010040-017DIATRIZOATE MEGLUMINE76%INJECTABLE / INJECTIONApproved before 1982c2088c7a36db…
2026-10-15 13:18:302026-09N010040-018CYSTOGRAFIN30%SOLUTION / URETHRALRLD, Approved before 1982c2088c7a36db…
2026-10-15 13:18:302026-09N010040-019RENOVIST II28.5%;29.1%INJECTABLE / INJECTIONApproved before 1982c2088c7a36db…
2026-10-15 13:18:302026-09N010040-020RENOVIST34.3%;35%INJECTABLE / INJECTIONApproved before 1982c2088c7a36db…
2026-10-15 13:18:302026-09N010040-021RENO-3030%SOLUTION / URETERALApproved before 1982c2088c7a36db…
2026-10-15 13:18:302026-09N010040-022CYSTOGRAFIN DILUTE18%SOLUTION / URETHRALRLD1982-11-09c2088c7a36db…
2026-09-14 22:38:342026-08N010040-001RENOGRAFIN-7666%;10%INJECTABLE / INJECTIONRLD, Approved before 198284e616aacf4f…
2026-09-14 22:38:342026-08N010040-006RENOGRAFIN-6052%;8%INJECTABLE / INJECTIONApproved before 198284e616aacf4f…
2026-09-14 22:38:342026-08N010040-012RENO-DIP30%INJECTABLE / INJECTIONApproved before 198284e616aacf4f…
2026-09-14 22:38:342026-08N010040-016RENO-6060%INJECTABLE / INJECTIONApproved before 198284e616aacf4f…
2026-09-14 22:38:342026-08N010040-017DIATRIZOATE MEGLUMINE76%INJECTABLE / INJECTIONApproved before 198284e616aacf4f…
2026-09-14 22:38:342026-08N010040-018CYSTOGRAFIN30%SOLUTION / URETHRALRLD, Approved before 198284e616aacf4f…
2026-09-14 22:38:342026-08N010040-019RENOVIST II28.5%;29.1%INJECTABLE / INJECTIONApproved before 198284e616aacf4f…
2026-09-14 22:38:342026-08N010040-020RENOVIST34.3%;35%INJECTABLE / INJECTIONApproved before 198284e616aacf4f…
2026-09-14 22:38:342026-08N010040-021RENO-3030%SOLUTION / URETERALApproved before 198284e616aacf4f…
2026-09-14 22:38:342026-08N010040-022CYSTOGRAFIN DILUTE18%SOLUTION / URETHRALRLD1982-11-0984e616aacf4f…
2026-08-18 06:07:402026-07N010040-001RENOGRAFIN-7666%;10%INJECTABLE / INJECTIONRLD, Approved before 1982caaa826d4ba7…
2026-08-18 06:07:402026-07N010040-006RENOGRAFIN-6052%;8%INJECTABLE / INJECTIONApproved before 1982caaa826d4ba7…
2026-08-18 06:07:402026-07N010040-012RENO-DIP30%INJECTABLE / INJECTIONApproved before 1982caaa826d4ba7…
2026-08-18 06:07:402026-07N010040-016RENO-6060%INJECTABLE / INJECTIONApproved before 1982caaa826d4ba7…
2026-08-18 06:07:402026-07N010040-017DIATRIZOATE MEGLUMINE76%INJECTABLE / INJECTIONApproved before 1982caaa826d4ba7…
2026-08-18 06:07:402026-07N010040-018CYSTOGRAFIN30%SOLUTION / URETHRALRLD, Approved before 1982caaa826d4ba7…
2026-08-18 06:07:402026-07N010040-019RENOVIST II28.5%;29.1%INJECTABLE / INJECTIONApproved before 1982caaa826d4ba7…
2026-08-18 06:07:402026-07N010040-020RENOVIST34.3%;35%INJECTABLE / INJECTIONApproved before 1982caaa826d4ba7…
2026-08-18 06:07:402026-07N010040-021RENO-3030%SOLUTION / URETERALApproved before 1982caaa826d4ba7…
2026-08-18 06:07:402026-07N010040-022CYSTOGRAFIN DILUTE18%SOLUTION / URETHRALRLD1982-11-09caaa826d4ba7…
2026-02-19 14:30 UTC2026-02N010040-001RENOGRAFIN-7666%;10%INJECTABLE / INJECTIONRLD, Approved before 1982011fe1cb6892…
2026-02-19 14:30 UTC2026-02N010040-006RENOGRAFIN-6052%;8%INJECTABLE / INJECTIONApproved before 1982011fe1cb6892…
2026-02-19 14:30 UTC2026-02N010040-012RENO-DIP30%INJECTABLE / INJECTIONApproved before 1982011fe1cb6892…
2026-02-19 14:30 UTC2026-02N010040-016RENO-6060%INJECTABLE / INJECTIONApproved before 1982011fe1cb6892…
2026-02-19 14:30 UTC2026-02N010040-017DIATRIZOATE MEGLUMINE76%INJECTABLE / INJECTIONApproved before 1982011fe1cb6892…
2026-02-19 14:30 UTC2026-02N010040-018CYSTOGRAFIN30%SOLUTION / URETHRALRLD, Approved before 1982011fe1cb6892…
2026-02-19 14:30 UTC2026-02N010040-019RENOVIST II28.5%;29.1%INJECTABLE / INJECTIONApproved before 1982011fe1cb6892…
2026-02-19 14:30 UTC2026-02N010040-020RENOVIST34.3%;35%INJECTABLE / INJECTIONApproved before 1982011fe1cb6892…
2026-02-19 14:30 UTC2026-02N010040-021RENO-3030%SOLUTION / URETERALApproved before 1982011fe1cb6892…
2026-02-19 14:30 UTC2026-02N010040-022CYSTOGRAFIN DILUTE18%SOLUTION / URETHRALRLD1982-11-09011fe1cb6892…

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
CystografinDIATRIZOATE MEGLUMINEBRACCO DIAGNOSTICS INC7496d736-9f7d-4136-ad5d-b24c7803c21b2025-11-23Warnings, Adverse reactionsExact identifier
ndc (package): 0270-0149-57
ndc (package): 0270-0149-60
ndc (product): 0270-0149
ndc11 (package): 00270014960
ndc11 (package): 00270014957
spl id: 6b067ea9-50b4-0ec7-1f1c-e07b00faced4
spl set id: 7496d736-9f7d-4136-ad5d-b24c7803c21b

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.