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 2 of 9 · 170 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Bacteriostatic WaterBACTERIOSTATIC WATERHospira, Inc.87d6e9dc-fe3b-4593-ac9a-d7493d1959c72026-05-22Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
WHITENING SUNSCREENANTI WRINKLEWHITENING SUNSCREENANTI WRINKLEShantou Oushiya Biotechnology Co.,Ltd524384e9-b3f8-4c13-e063-6394a90a89732026-05-20WarningsExact identifier
unii: 059QF0KO0R
Sterile WaterWATERHospira, Inc.3a6422e1-feee-4095-8883-2b0837039e6e2026-05-07Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
Multi FlowerAESCULUS CARNEA, FLOS, AESCULUS HIPPOCASTANUM, FLOS, AGRIMONIA EUPATORIA, FLOS, BROMUS RAMOSUS, FLOS, CALLUNA VULGARIS, FLOS, CARPINUS BETULUS , FLOS, CASTANEA SATIVA, FLOS, CENTAURIUM UMBELLATUM, FLOS, CERATOSTIGMA WILLMOTTIANUM, FLOS, CICHORIUM INTYBUS, FLOS, CLEMATIS VITALBA, FLOS, CLEMATIS VITALBA, FLOS, FAGUS SYLVATICA, FLOS, GENTIANELLA AMARELLA, FLOS, HELIANTHEMUM NUMMULARIUM, FLOS, ILEX AQUIFOLIUM, FLOS, IMPATIENS GLANDULIFERA, FLOS, LARIX DECIDUA, FLOS, LONICERA CAPRIFOLIUM, FLOSEnergique, Inc.09c059e7-f748-402c-8447-af5b61169c582026-05-06WarningsExact identifier
unii: 059QF0KO0R
CLARISCANGADOTERATE MEGLUMINEGE Healthcarec9e273b3-481f-4899-8913-95aaddcc76622026-04-30Boxed warning, Warnings, Adverse reactionsExact identifier
unii: L0ND3981AG
CLARISCANGADOTERATE MEGLUMINEGE Healthcare6f8c9fac-c995-4bf4-950d-ab89deb291b52026-04-29Boxed warning, Warnings, Adverse reactionsExact identifier
unii: L0ND3981AG
KIDS TOOTHPASTE, FOR CAVITY PROTECTIONKIDS TOOTHPASTE FOR CAVITY PROTECTIONShulisa (Foshan) Daily ChemicalIndustry Co., Ltd4e8fab9e-f05c-5e2f-e063-6294a90aecf92026-04-03WarningsExact identifier
unii: 059QF0KO0R
Sterile WaterWATERHospira, Inc.2b9ea23a-f9e9-48a8-25b7-519e3bbd68282026-03-18Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
TINTED SUNSCREEN FOUNDATIONTINTED SUNSCREEN FOUNDATIONGuanghzou AiXin Biotech Co Ltd396393c4-b50c-3877-e063-6294a90a0e9b2026-03-17WarningsExact identifier
unii: 059QF0KO0R
2-Pack Facial Serum2-PACK FACIAL SERUMGuangzhou Ariel Biotech Co., Ltd.27c7f645-cfb3-6db1-e063-6394a90a42ff2026-03-06WarningsExact identifier
unii: 059QF0KO0R
INSULIN DILUTING MEDIUM FOR KirstyWATERBiocon Biologics Inc.3db1d482-7e1f-aec6-79ef-3f305b4d82772026-01-20Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
Walgreens Sterile Soothing Eye WashPURIFIED WATERWalgreensa62e3294-abd6-48dc-81b1-62a809bdc9682026-01-14WarningsExact identifier
unii: 059QF0KO0R
Plus Rinse Emergency EyewashPURIFIED WATERINNOVATIVE SAFETY SUPPLY INC.b3f47d26-39e4-4aea-bb92-358def52b6522026-01-08WarningsExact identifier
unii: 059QF0KO0R
pH Neutral Emergency EyewashWATERINNOVATIVE SAFETY SUPPLY INC.29a1bd1e-d0dd-478f-e063-6394a90ab0aa2026-01-08WarningsExact identifier
unii: 059QF0KO0R
Eye CleanEYE WASHHART Health41f53e2e-c2bc-4bf1-a541-3bcb2cf630022025-12-31WarningsExact identifier
unii: 059QF0KO0R
teeth and gumsCALC FLUORICA, CALC PHOS, FERRUM PHOS, KALI PHOS, MAG PHOS, MALUS PUMILA, FLOS, ROCK WATER, ULEX EUROPAEUS, FLOSSiddha Flower Essences LLC926c79d5-d270-4c0d-aca9-b58571c24f3a2025-12-31WarningsExact identifier
unii: 059QF0KO0R
lung and sinusCALC PHOS, FERRUM PHOS, GENTIANELLA AMARELLA, FLOS, KALI MUR, KALI PHOS, KALI SULPH, ROCK WATER, ROSE CANINA, FLOSSiddha Flower Essences LLC9f7c949f-21bc-473c-ab8d-24837893fccc2025-12-31WarningsExact identifier
unii: 059QF0KO0R
Quality Choice Eye WashWATERChain Drug Marketing Assoc., Inc.1fb8a109-351b-7039-e063-6394a90a73112025-12-30WarningsExact identifier
unii: 059QF0KO0R
Rite Aid Eye WashPURIFIED WATERRite Aid28a18e04-d735-a511-e063-6394a90af6bb2025-12-30WarningsExact identifier
unii: 059QF0KO0R
OCUFRESHWATEROptics Laboratory Inc.b8e477a9-66b9-496b-92fb-3d4bbd7b36b52025-12-29WarningsExact identifier
unii: 059QF0KO0R

Reported adverse events (FAERS/openFDA)#

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