NDC 0019-3183-07 - Conray 43

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
0019-3183
Requested NDC
0019-3183-07
Package NDCs from labels
0019-3183-09, 0019-3183-50, 0019-3183-15, 0019-3183-05, 0019-3183-07
Manufacturer
Liebel-Flarsheim Company LLC | Justesa Imagen, S.A.U.
Effective date
2019-06-27
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
August 2017 Conray ® 43 [Iothalamate Meglumine Injection USP 43%] Rx onlyLiebel-Flarsheim Company LLC | Justesa Imagen, S.A.U.2019-06-27HUMAN PRESCRIPTION DRUG LABEL
National Council for Prescription Drug Programs indexing - billing unitNational Council for Prescription Drug Programs2012-07-24Indexing - Billing Unit

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0019-3183-05ML - Milliliter0019-3183eac9e807-8c57-4d2b-acad-633ed65cd88412019-02-13
0019-3183-07ML - Milliliter0019-318372b62f7e-35e0-49be-b70d-5d0f2976f8a012012-07-24
0019-3183-09ML - Milliliter0019-318314595e8a-426a-40c1-8a65-208c7b3bdbed12012-07-24
0019-3183-11ML - Milliliter0019-318390220578-a58c-4a24-9cad-fee07e38aa1212012-07-24
0019-3183-15ML - Milliliter0019-3183072f48ca-b80b-48f5-aa0c-bebde8a10fcf12012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
IOTHALAMATE MEGLUMINEACTIVE INGREDIENTXUW72GOP7WCONRAY 43 (IOTHALAMATE MEGLUMINE) INJECTION [MALLINCKRODT INC.]9
IOTHALAMIC ACIDACTIVE MOIETY16CHD79MIXCONRAY 43 (IOTHALAMATE MEGLUMINE) INJECTION [MALLINCKRODT INC.]9
EDETATE CALCIUM DISODIUMINACTIVE INGREDIENT25IH6R4SGFCONRAY 43 (IOTHALAMATE MEGLUMINE) INJECTION [MALLINCKRODT INC.]9
SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORMINACTIVE INGREDIENT3980JIH2SWCONRAY 43 (IOTHALAMATE MEGLUMINE) INJECTION [MALLINCKRODT INC.]9

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 2 of 2 · 28 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
FleetSODIUM PHOSPHATE, DIBASIC AND SODIUM PHOSPHATE, MONOBASICC.B. Fleet Company, Inc.f50ba829-16c3-40a7-9822-8d6d00353b332024-02-29WarningsExact identifier
unii: 3980JIH2SW
Cysto-Conray IIIOTHALAMATE MEGLUMINELiebel-Flarsheim Company LLC8841ab4d-674d-4beb-88a5-13e35f6005cc2020-12-31Boxed warning, Warnings, Adverse reactionsExact identifier
unii: XUW72GOP7W
ee608418-2b2a-47d8-84e2-9f2ae1be04aa77dd7fb3-18c4-4acb-af07-f929dff039032020-12-08Boxed warning, Warnings, Adverse reactionsExact identifier
spl set id: 77dd7fb3-18c4-4acb-af07-f929dff03903
FREDS SALINE TWIN PACK LAXATIVESODIUM PHOSPHATE, DIBASIC, UNSPECIFIED FORM AND SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORMFRED'S7d15057f-eb3b-477f-ab14-68c3c38ea9102018-12-26WarningsExact identifier
unii: 3980JIH2SW
Marcs Twin PackSODIUM PHOSPHATE, DIBASIC, UNSPECIFIED FORM AND SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORMMarc Glassman Inc.66348ee5-803a-4b78-94dd-55bc9d3543c32018-07-10WarningsExact identifier
unii: 3980JIH2SW
QUALITY CHOICE SINGLE SALINE LAXATIVESODIUM PHOSPHATE, DIBASIC, UNSPECIFIED FORM AND SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORMAlcyon Health, LLC.eb499c7f-9c7b-4097-83a3-82aabffd6beb2017-07-12WarningsExact identifier
unii: 3980JIH2SW
Pro-Enema Single Saline LaxativeSODIUM PHOSPHATE, DIBASIC AND SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORMPropharma Medical Suppliese53c5eda-21da-4aed-a592-315100167cc22017-06-08WarningsExact identifier
unii: 3980JIH2SW
Saline Laxative Cherry LaxativeSODIUM PHOSPHATE, DIBASIC AND SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORMDolgencorp Inc.ca3c00d9-4301-4de8-94f5-34f1bcc761ab2017-04-13WarningsExact identifier
unii: 3980JIH2SW

Reported adverse events (FAERS/openFDA)#

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