NDC 0024-4142-18 - Multaq

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: 0024-4142
Requested NDC: 0024-4142-18
Package NDCs from labels: 0024-4142-60, 0024-4142-50, 0024-4142-10, 0024-4142-00, 0024-4142-06, 0024-4142-18
Manufacturer: Cardinal Health 107, LLC
Effective date: 2026-01-27
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Multaq - Cardinal Health 107, LLC	Cardinal Health 107, LLC	2026-01-27	HUMAN PRESCRIPTION DRUG LABEL
Multaq - Sanofi-Aventis U.S. LLC \| Sanofi Winthrop Industrie \| Genzyme Corporation	Sanofi-Aventis U.S. LLC \| Sanofi Winthrop Industrie \| Genzyme Corporation	2025-05-29	HUMAN PRESCRIPTION DRUG LABEL
Multaq - Physicians Total Care, Inc.	Physicians Total Care, Inc.	2011-12-28	HUMAN PRESCRIPTION DRUG LABEL
National Council for Prescription Drug Programs indexing - billing unit	National Council for Prescription Drug Programs	2012-07-24	Indexing - Billing Unit

FDA-Initiated Inactive NDC Indexing#

NDC, Related label table
NDC	Related label
0024-4142-06	These highlights do not include all the information needed to use MULTAQ safely and effectively. See full prescribing information for MULTAQ. MULTAQ® (dronedarone) tablets, for oral use Initial U.S. Approval: 2009
0024-4142-10	These highlights do not include all the information needed to use MULTAQ safely and effectively. See full prescribing information for MULTAQ. MULTAQ® (dronedarone) tablets, for oral use Initial U.S. Approval: 2009
0024-4142-50	These highlights do not include all the information needed to use MULTAQ safely and effectively. See full prescribing information for MULTAQ. MULTAQ® (dronedarone) tablets, for oral use Initial U.S. Approval: 2009
0024-4142-60	These highlights do not include all the information needed to use MULTAQ safely and effectively. See full prescribing information for MULTAQ. MULTAQ® (dronedarone) tablets, for oral use Initial U.S. Approval: 2009

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
0024-4142-00	Multaq	6 in 1 BLISTER PACK	TABLET, FILM COATED	6	37
0024-4142-06	Multaq	8 in 1 BOX	TABLET, FILM COATED	8	37
0024-4142-10	Multaq	10 in 1 BLISTER PACK	TABLET, FILM COATED	10	37
0024-4142-10	Multaq	10 in 1 BOX	TABLET, FILM COATED	10	37
0024-4142-50	Multaq	500 in 1 BOTTLE	TABLET, FILM COATED	500	37
0024-4142-60	Multaq	60 in 1 BOTTLE	TABLET, FILM COATED	60	37

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0024-4142	MULTAQ (DRONEDARONE) TABLET, FILM COATED [SANOFI-AVENTIS U.S. LLC]	36	Current NDC, Legacy NDC, 6 package rows	20240602_7fa41601-7fb5-4155-8e50-2ae903f0d2d6.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
0024-4142-10	EA - Each	0024-4142	7c134bb2-6e52-4a0e-b506-64bb2eaeecb7	1	2012-07-24
0024-4142-18	EA - Each	0024-4142	466da1e2-de71-4365-a2b2-17751642590d	1	2012-07-24
0024-4142-60	EA - Each	0024-4142	52f55635-5110-4c6d-9073-889d51459120	1	2012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
Dronedarone	ACTIVE INGREDIENT	JQZ1L091Y2	MULTAQ (DRONEDARONE) TABLET, FILM COATED [SANOFI-AVENTIS U.S. LLC]	22
Dronedarone	ACTIVE MOIETY	JQZ1L091Y2	MULTAQ (DRONEDARONE) TABLET, FILM COATED [SANOFI-AVENTIS U.S. LLC]	22
carnauba wax	INACTIVE INGREDIENT	R12CBM0EIZ	MULTAQ (DRONEDARONE) TABLET, FILM COATED [SANOFI-AVENTIS U.S. LLC]	22
crospovidone	INACTIVE INGREDIENT	68401960MK	MULTAQ (DRONEDARONE) TABLET, FILM COATED [SANOFI-AVENTIS U.S. LLC]	22
hypromelloses	INACTIVE INGREDIENT	3NXW29V3WO	MULTAQ (DRONEDARONE) TABLET, FILM COATED [SANOFI-AVENTIS U.S. LLC]	22
lactose monohydrate	INACTIVE INGREDIENT	EWQ57Q8I5X	MULTAQ (DRONEDARONE) TABLET, FILM COATED [SANOFI-AVENTIS U.S. LLC]	22
magnesium stearate	INACTIVE INGREDIENT	70097M6I30	MULTAQ (DRONEDARONE) TABLET, FILM COATED [SANOFI-AVENTIS U.S. LLC]	22
poloxamer 407	INACTIVE INGREDIENT	TUF2IVW3M2	MULTAQ (DRONEDARONE) TABLET, FILM COATED [SANOFI-AVENTIS U.S. LLC]	22
polyethylene glycol 6000	INACTIVE INGREDIENT	30IQX730WE	MULTAQ (DRONEDARONE) TABLET, FILM COATED [SANOFI-AVENTIS U.S. LLC]	22
silicon dioxide	INACTIVE INGREDIENT	ETJ7Z6XBU4	MULTAQ (DRONEDARONE) TABLET, FILM COATED [SANOFI-AVENTIS U.S. LLC]	22
starch, corn	INACTIVE INGREDIENT	O8232NY3SJ	MULTAQ (DRONEDARONE) TABLET, FILM COATED [SANOFI-AVENTIS U.S. LLC]	22
titanium dioxide	INACTIVE INGREDIENT	15FIX9V2JP	MULTAQ (DRONEDARONE) TABLET, FILM COATED [SANOFI-AVENTIS U.S. LLC]	22
Dronedarone	ACTIVE INGREDIENT	JQZ1L091Y2	MULTAQ (DRONEDARONE) TABLET, FILM COATED [CARDINAL HEALTH]	3
Dronedarone	ACTIVE MOIETY	JQZ1L091Y2	MULTAQ (DRONEDARONE) TABLET, FILM COATED [CARDINAL HEALTH]	3
carnauba wax	INACTIVE INGREDIENT	R12CBM0EIZ	MULTAQ (DRONEDARONE) TABLET, FILM COATED [CARDINAL HEALTH]	3
crospovidone	INACTIVE INGREDIENT	68401960MK	MULTAQ (DRONEDARONE) TABLET, FILM COATED [CARDINAL HEALTH]	3
hypromelloses	INACTIVE INGREDIENT	3NXW29V3WO	MULTAQ (DRONEDARONE) TABLET, FILM COATED [CARDINAL HEALTH]	3
lactose monohydrate	INACTIVE INGREDIENT	EWQ57Q8I5X	MULTAQ (DRONEDARONE) TABLET, FILM COATED [CARDINAL HEALTH]	3
magnesium stearate	INACTIVE INGREDIENT	70097M6I30	MULTAQ (DRONEDARONE) TABLET, FILM COATED [CARDINAL HEALTH]	3
poloxamer 407	INACTIVE INGREDIENT	TUF2IVW3M2	MULTAQ (DRONEDARONE) TABLET, FILM COATED [CARDINAL HEALTH]	3
polyethylene glycol 6000	INACTIVE INGREDIENT	30IQX730WE	MULTAQ (DRONEDARONE) TABLET, FILM COATED [CARDINAL HEALTH]	3
silicon dioxide	INACTIVE INGREDIENT	ETJ7Z6XBU4	MULTAQ (DRONEDARONE) TABLET, FILM COATED [CARDINAL HEALTH]	3
starch, corn	INACTIVE INGREDIENT	O8232NY3SJ	MULTAQ (DRONEDARONE) TABLET, FILM COATED [CARDINAL HEALTH]	3
titanium dioxide	INACTIVE INGREDIENT	15FIX9V2JP	MULTAQ (DRONEDARONE) TABLET, FILM COATED [CARDINAL HEALTH]	3
Dronedarone	ACTIVE INGREDIENT	JQZ1L091Y2	MULTAQ (DRONEDARONE) TABLET, FILM COATED [PHYSICIANS TOTAL CARE, INC.]	2
Dronedarone	ACTIVE MOIETY	JQZ1L091Y2	MULTAQ (DRONEDARONE) TABLET, FILM COATED [PHYSICIANS TOTAL CARE, INC.]	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 8 of 130 · 2,595 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
SkinCeuticals Future Mineral UV Defense Invisble Sunscreen Mineral Filters Broad Spectrum SPF 50	TITANIUM DIOXIDE AND ZINC OXIDE	L'Oreal USA Products Inc	0b92a940-0dd4-4266-bd47-88c27def62c0	2026-05-20	Warnings	Exact identifier unii: 15FIX9V2JP
WHITENING SUNSCREENANTI WRINKLE	WHITENING SUNSCREENANTI WRINKLE	Shantou Oushiya Biotechnology Co.,Ltd	524384e9-b3f8-4c13-e063-6394a90a8973	2026-05-20	Warnings	Exact identifier unii: 15FIX9V2JP
IT COSMETICS HELLO SUNSHINE Invisible Sunscreen Broad Spectrum SPF 50 UVA UVB Mineral 50	TITANIUM DIOXIDE AND ZINC OXIDE	L'Oreal USA Products Inc.	fded7dfb-ffb9-4fb0-9511-273e0e126969	2026-05-20	Warnings	Exact identifier unii: 15FIX9V2JP
Freaks of Nature Peak Performance Broad Spectrum SPF 50	FREAKS OF NATURE PEAK PERFORMANCE BROAD SPECTRUM SPF 50	THE FREAKS OF NATURE, INC.	5247187d-a14c-6468-e063-6394a90ace3e	2026-05-20	Warnings	Exact identifier unii: 15FIX9V2JP
Dentaforce	ANTIMONIUM CRUDUM, BELLADONNA, CALCAREA CARBONICA, CALCAREA FLUORICA, CALCAREA PHOSPHORICA, HEKLA LAVA, MERCURIUS SOLUBILIS, PLUMBUM METALLICUM, SEPIA, SILICEA, HYDROFLUORICUM ACIDUM	BioActive Nutritional, Inc.	82321547-e04a-42ff-aa39-6a192638e5a2	2026-05-18	Warnings	Exact identifier unii: ETJ7Z6XBU4
LANCOME PARIS UV EXPERT SUPRA SCREEN MINERAL INVISIBLE SUNSCREEN SPF 50 SERUM	TITANIUM DIOXIDE AND ZINC OXIDE	LOreal USA Products Inc.	23cc5ff4-f842-4e3e-ac5c-23dbaf7d3914	2026-05-15	Warnings	Exact identifier unii: 15FIX9V2JP
LANCOME PARIS UV EXPERT SUPRA SCREEN MINERAL INVISIBLE SUNSCREEN SPF 50 SERUM	TITANIUM DIOXIDE AND ZINC OXIDE	SICOS ET CIE	c688f8e6-2cd2-40db-b03f-90fd74c2d89c	2026-05-15	Warnings	Exact identifier unii: 15FIX9V2JP
Lancome Paris Teint Idole Ultra Wear Breathable Coverage Foundation Broad Spectrum SPF 25 Sunscreen	OCTINOXATE AND TITANIUM DIOXIDE	L'Oreal USA Products Inc	7df9dbd2-7db9-4961-819d-e93d14a065c3	2026-05-15	Warnings	Exact identifier unii: 15FIX9V2JP
Lancome Paris Teint Idole Ultra Wear Breathable Coverage Foundation Broad Spectrum SPF 25 Sunscreen	OCTINOXATE AND TITANIUM DIOXIDE	SICOS ET CIE	20efd5fa-3077-4fd4-82d0-ddca946e4528	2026-05-15	Warnings	Exact identifier unii: 15FIX9V2JP
MELAO Hydrating Lightweight Sunscreen	OCTOCRYLENE,HOMOSALATE,ETHYLHEXYL SALICYLATE,PHENYLBENZIMIDAZOLE SULFONIC ACID,BUTYL METHOXYDIBENZOYLMETHANE,TITANIUM DIOXIDE	Guangdong Aimu Biological Technology Co., Ltd	51c353cb-94c4-e110-e063-6394a90a497e	2026-05-14	Warnings	Exact identifier unii: 15FIX9V2JP
C07 STRONG LIGAMENTS AND JOINTS	ARNICA MONTANA, ASCORBICUM ACIDUM, BOS TAURUS LYMPH VESSEL, INTERVERTEBRAL FIBROCARTILAGE, BOS TAURUS MESENCHYME, CALCAREA PHOSPHORICA, CARTILAGO SUIS, FORMICUM ACIDUM, LAPIS ALBUS, PINUS MONTANA LEAFY TWIG, RHAMNUS CALIFORNICA, RHUS TOXICODENDRON, RUTA GRAVEOLENS, SILICEA, SUS SCROFA JOINT ENVELOPE, SUS SCROFA LIGAMENT, SUS SCROFA MENISCUS, SUS SCROFA PARATHYROID GLAND, SUS SCROFA VEIN, SYMPHYTUM OFFICINALE	Apex Energetics Inc.	bccf8c83-a6cd-e58c-e053-2a95a90a43d7	2026-05-13	Warnings	Exact identifier unii: ETJ7Z6XBU4
Even Tone Mineral Sunscreen Broad Spectrum SPF 36 Medium - Dark	TITANIUM DIOXIDE AND ZINC OXIDE	SENT, Inc.	aedde765-931f-430e-9fc3-d87bde2b78cd	2026-05-12	Warnings	Exact identifier unii: 15FIX9V2JP
Even Tone Mineral Sunscreen Broad Spectrum SPF 40 Light - Medium	TITANIUM DIOXIDE AND ZINC OXIDE	SENT, Inc.	417305d7-d32e-4bc9-8f77-0a42b6bdecf5	2026-05-12	Warnings	Exact identifier unii: 15FIX9V2JP
The Perfect Derma Mineral Perfection Broad Spectrum SPF 30	TITANIUM DIOXIDE, ZINC OXIDE	Bella Medical Products LLC	518f69fc-fd39-8195-e063-6294a90a3fdd	2026-05-11	Warnings	Exact identifier unii: 15FIX9V2JP
Radical Rescue Morning UVA/UVB Defense Primer Broad Spectrum SPF 30 Universal Tint Mineral Sunscreen	RADICAL RESCUE SPF 30 MINERAL SUNSCREEN	ProTransit, Inc.	38e0139c-bb87-55ba-e063-6294a90a82ee	2026-05-11	Warnings	Exact identifier unii: 15FIX9V2JP
EELHOE Sunscreen	TITANIUM DIOXIDE	Shantou Eelhoe Daily Chemical Technology Co., Ltd.	5196ccb0-4515-7e40-e063-6394a90a09bd	2026-05-11	Warnings	Exact identifier unii: 15FIX9V2JP
Acne Relief	BELLADONNA, SILICEA, GRAPHITES, HEPAR SULPHURIS CALCAREUM, KALI BROMATUM, LEDUM PALUSTRE, NATRUM MURIATICUM, SELENIUM, SULPHUR	NaturalCare	487b1373-b78c-4510-964a-6ab0fe781ff4	2026-05-08	Warnings	Exact identifier unii: ETJ7Z6XBU4
Dior Backstage Glow-Up Skin Tint Tinted Moisturizer SPF 20 5.5N Neutral	OCTISALATE, TITANIUM DIOXIDE	Parfums Christian Dior	bb65c8d7-318f-4d52-9d74-ca22ce389638	2026-05-07	Warnings	Exact identifier unii: 15FIX9V2JP
Dior Backstage Glow-Up Skin Tint Tinted Moisturizer SPF 20 4.5N Neutral	OCTISALATE, TITANIUM DIOXIDE	Parfums Christian Dior	67b90f00-4c82-40cd-af96-f8dedf95f8af	2026-05-06	Warnings	Exact identifier unii: 15FIX9V2JP
Dior Backstage Glow-Up Skin Tint Tinted Moisturizer SPF 20 4W Warm	OCTISALATE, TITANIUM DIOXIDE	Parfums Christian Dior	7a2bd17d-0ea7-4326-9939-a747869c01d2	2026-05-06	Warnings	Exact identifier unii: 15FIX9V2JP

Reported adverse events (FAERS/openFDA)#

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