NDC 67684-2000-01 - DOTAREM

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
67684-2000
Requested NDC
67684-2000-01
Package NDCs from labels
67684-2000-1, 67684-2000-0, 67684-2000-2, 67684-2000-3, 67684-2000-5, 67684-2000-6, 67684-2000-7, 67684-2000-4, 67684-2000-01
Manufacturer
Guerbet LLC | Recipharm Monts | Simafex | PCAS Finland O.y | Liebel-Flarsheim Company LLC
Effective date
2025-03-14
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
DOTAREM - Guerbet LLC | Recipharm Monts | Simafex | PCAS Finland O.y | Liebel-Flarsheim Company LLCGuerbet LLC | Recipharm Monts | Simafex | PCAS Finland O.y | Liebel-Flarsheim Company LLC2025-03-14HUMAN PRESCRIPTION DRUG LABEL
DOTAREM - Guerbet LLC | Recipharm | Simafex | PCAS Finland O.y | Liebel-Flarsheim Company LLCGuerbet LLC | Recipharm | Simafex | PCAS Finland O.y | Liebel-Flarsheim Company LLC2025-03-12HUMAN PRESCRIPTION DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
67684-2000-0DOTAREM10 in 1 PACKAGEINJECTION1025
67684-2000-0DOTAREM5 mL in 1 VIALINJECTION525
67684-2000-1DOTAREM10 mL in 1 VIALINJECTION1025
67684-2000-1DOTAREM10 in 1 PACKAGEINJECTION1025
67684-2000-2DOTAREM10 in 1 PACKAGEINJECTION1025
67684-2000-2DOTAREM15 mL in 1 VIALINJECTION1525
67684-2000-3DOTAREM20 mL in 1 VIALINJECTION2025
67684-2000-3DOTAREM10 in 1 PACKAGEINJECTION1025
67684-2000-5DOTAREM5 in 1 PACKAGEINJECTION525
67684-2000-5DOTAREM10 mL in 1 SYRINGEINJECTION1025
67684-2000-6DOTAREM15 mL in 1 SYRINGEINJECTION1525
67684-2000-6DOTAREM5 in 1 PACKAGEINJECTION525
67684-2000-7DOTAREM20 mL in 1 SYRINGEINJECTION2025
67684-2000-7DOTAREM5 in 1 PACKAGEINJECTION525
67684-2000-4DOTAREM6 in 1 PACKAGEInjection617
67684-2000-4DOTAREM100 mL in 1 VIALInjection10017

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
67684-2000DOTAREM (GADOTERATE MEGLUMINE) INJECTION [GUERBET LLC]25Current NDC, Legacy NDC, 14 package rows20250321_e2c4a5ac-2df2-4cf4-a2d3-6fbe2d898ebc.zip
67684-2000DOTAREM (GADOTERATE MEGLUMINE) INJECTION [GUERBET LLC]17Current NDC, Legacy NDC, 2 package rows20250321_82b83e61-6af8-4225-aa39-8cbf206f65b0.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
67684-2000-0ML - Milliliter67684-200037f15795-d63f-460a-9206-c5c0da62856412019-01-24
67684-2000-1ML - Milliliter67684-20003016fd32-3e7d-4b63-ba2c-b9a9e3d6d79f12013-09-04
67684-2000-2ML - Milliliter67684-2000d47ebf69-7683-4f57-9b86-2abf8caf6d7212013-09-04
67684-2000-3ML - Milliliter67684-2000b3ecd5e5-11e1-43da-876e-5c5f327e2b0912013-09-04
67684-2000-4ML - Milliliter67684-20006b70e2f1-b672-4e34-82fa-30c23d0c3eca12013-09-04
67684-2000-5ML - Milliliter67684-20002664bf82-741c-4f1e-b761-f9d56049b77f12013-10-17
67684-2000-6ML - Milliliter67684-20003c7eb227-6a12-449b-ae4c-9919aa3b918712013-10-17
67684-2000-7ML - Milliliter67684-2000a6a6a298-2b05-46fe-8f1d-a7f06160918e12013-10-17

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
gadoterate meglumineACTIVE INGREDIENTL0ND3981AGDOTAREM (GADOTERATE MEGLUMINE) INJECTION [GUERBET LLC]3
GADOLINIUM CATION (3+)ACTIVE MOIETYAZV954TZ9NDOTAREM (GADOTERATE MEGLUMINE) INJECTION [GUERBET LLC]3
WATERINACTIVE INGREDIENT059QF0KO0RDOTAREM (GADOTERATE MEGLUMINE) INJECTION [GUERBET LLC]3
gadoterate meglumineACTIVE INGREDIENTL0ND3981AGDOTAREM (GADOTERATE MEGLUMINE) INJECTION [GUERBET LLC]2
GADOLINIUM CATION (3+)ACTIVE MOIETYAZV954TZ9NDOTAREM (GADOTERATE MEGLUMINE) INJECTION [GUERBET LLC]2
WATERINACTIVE INGREDIENT059QF0KO0RDOTAREM (GADOTERATE MEGLUMINE) INJECTION [GUERBET LLC]2

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 9 of 9 · 169 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
EyewashEYEWASHGlobal Equipment Companyc4f78121-4668-2e0c-e053-2995a90ab6c62021-06-17WarningsExact identifier
unii: 059QF0KO0R
Sterile WaterWATERAsclemed USA, Inc.45c38269-883c-4198-a9d5-03810a4420ec2021-01-14Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
Bach Original Flower RemediesWATERNelson Bach USA Limited09c76050-42c5-4403-865c-a1f6f668d9c02020-06-15WarningsExact identifier
unii: 059QF0KO0R
Sterile WaterWATERBaxter Healthcare Company8bcf5572-49e1-4302-9522-56f57904cb4a2019-12-29Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
Dynamic Eyewash with EyecupWATERDynamic Safety International7d3af0f4-0e1f-9ea5-e053-2991aa0af7a22018-12-17WarningsExact identifier
unii: 059QF0KO0R
Bio Rock WaterROCK WATERBioActive Nutritional, Inc.178bd16d-0d4f-49d8-866b-8ab3a3c6889d2018-07-30WarningsExact identifier
unii: 059QF0KO0R
Sterile WaterWATERBaxter Healthcare Corporationef3e79c5-3f58-4b36-a296-64b7d9a651c12017-10-17Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
Eye WashWATERCVS Pharmacy049cee29-7ec2-4d5b-8308-f522acde43a72017-03-29WarningsExact identifier
unii: 059QF0KO0R
Sterile WaterWATERBaxter Healthcare Company210dc9ab-d6ca-4552-ac19-1be17792d2902016-05-31Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R

Reported adverse events (FAERS/openFDA)#

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