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 1 of 133 · 2,643 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Lymph Tonic II	ECHINACEA (ANGUSTIFOLIA), COLLINSONIA CANADENSIS, PHYTOLACCA DECANDRA, KALI IODATUM, PINUS SYLVESTRIS, PIX LIQUIDA, FERRUM PHOSPHORICUM, AESCULUS HIPPOCASTANUM, BARYTA CARBONICA, BERBERIS VULGARIS, CALCAREA CARBONICA, CALCAREA PHOSPHORICA, CAUSTICUM, HEPAR SULPHURIS CALCAREUM, KREOSOTUM, LYCOPODIUM CLAVATUM, MERCURIUS SOLUBILIS, NATRUM MURIATICUM, NITRICUM ACIDUM, PHOSPHORUS, PULSATILLA (PRATENSIS), SILICEA, STELLARIA MEDIA, SULPHUR, TEREBINTHINA, THUJA OCCIDENTALIS, BUFO RANA	BioActive Nutritional, Inc.	0e3265b0-b210-4a4c-80d2-8a9712981d4e	2026-09-17	Warnings	Exact identifier unii: ETJ7Z6XBU4
Stay Ageless Tinted Mineral Sunscreen	BROAD SPECTRUM SPF30	W Aesthetics	5b0f2c8f-d6fa-5e25-e063-6394a90a084d	2026-09-09	Warnings	Exact identifier unii: 15FIX9V2JP
Psoriasis Control	CENTELLA ASIATICA, SODIUM CHLORIDE, AND SILICON DIOXIDE	Forces of Nature	2db33771-0bb9-49f8-84fa-dddc28e4ba26	2026-09-04	Warnings	Exact identifier unii: ETJ7Z6XBU4
BMNP Silicea	SILICEA	Total Operations Management LLC DBA:Bestmade Natural Products Micro	5a58454f-aed6-24ba-e063-6294a90a47fb	2026-08-31	Warnings	Exact identifier unii: ETJ7Z6XBU4
MZANK SUNSCREEN DAILY ULTIMATE PROTECTION SPF50	SUNSCREEN SPF50	Guangzhou Meixi Biotechnology Co., Ltd.	5a0b4bd2-f6ad-35dc-e063-6294a90a8a66	2026-08-27	Warnings	Exact identifier unii: 15FIX9V2JP
MELAO Hydrating Lightweight Sunscreen	AVOBENZONE,ENSULIZOLE,HOMOSALATE,OCTISALATE,OCTOCRYLENE,TITANIUM DIOXIDE	Guangdong Aimu Biological Technology Co., Ltd	59eeaea1-d726-99f3-e063-6394a90aeea3	2026-08-26	Warnings	Exact identifier unii: 15FIX9V2JP
Argentum Quartz	ARGENTUM QUARTZ	Uriel Pharmacy Inc.	765c8c8f-0727-45da-a77e-c3907a3d0793	2026-08-26	Warnings	Exact identifier unii: ETJ7Z6XBU4
Endometrium Argentum	ENDOMETRIUM ARGENTUM	Uriel Pharmacy Inc	d2d1428a-c8b5-9529-e053-2995a90a2343	2026-08-26	Warnings	Exact identifier unii: ETJ7Z6XBU4
S12 AIRBORNE	ALFALFA, ALLIUM SATIVUM, ARSENICUM IODATUM, BARLEY, BETULA PUBESCENS, BROWN RICE, CORN GRAIN, EUPHRASIA OFFICINALIS, FEATHER MIX, HAIR MIX, HISTAMINUM, HOUSE DUST MITE, LOLIUM PERENNE, OAT, PERFOLIATE HONEYSUCKLE, PHLEUM PRATENSE, POLLEN MIX, RYE, SABADILLA, SILICEA, SKIN MIX, SOLIDAGO VIRGAUREA, TARAXACUM OFFICINALE, TEREBINTHINA, WHEAT	Apex Energetics Inc.	bb0036c3-1e4d-5750-e053-2995a90ae895	2026-08-26	Warnings	Exact identifier unii: ETJ7Z6XBU4
Q Skin Science	SUNSCREEN	International Cosmeceuticals, Inc	59e4c3d0-ee4c-2350-e063-6394a90ac9d2	2026-08-25	Warnings	Exact identifier unii: 15FIX9V2JP
MELAO zinc stick(GREEN)	TITANIUM DIOXIDE,ZINC OXIDE,OCTOCRYLENE	Guangzhou Haishi Biological Technology Co., Ltd.	59c70c82-f7ff-9a04-e063-6294a90a7b3d	2026-08-24	Warnings	Exact identifier unii: 15FIX9V2JP
SKIN-INFUSED FOUNDATION SPF 25/ Mineral sunscreen broad Spectrum SPF 25 01	ZINC OXIDE, TITANIUM DIOXIDE	Cosmuses Cosmetics (Ningbo) Co., Ltd.	59d74e3f-e3fa-a7a9-e063-6294a90a76e5	2026-08-24	Warnings	Exact identifier unii: 15FIX9V2JP
Aging Eye Formula	CINERARIA MARITIMA, EYE (SUIS), CALCAREA FLUORICA, CAUSTICUM, PHOSPHORUS, SILICEA, ZINCUM METALLICUM, GERMANIUM METALLICUM, NATRUM MURIATICUM	Nutritional Specialties, Inc.	d5b44f79-5299-4b31-ba45-0e511cdbe17c	2026-08-24	Warnings	Exact identifier unii: ETJ7Z6XBU4
Rohto All-In-One	HYPROMELLOSE, TETRAHYDROZOLINE HYDROCHLORIDE, ZINC SULFATE	The Mentholatum Company	43e690e4-b381-46e3-838c-33aef5bdadde	2026-08-20	Warnings	Exact identifier unii: 3NXW29V3WO
Bio Combination 28	SCHUESSLER SALTS	LDD Bioscience Private Limited	597caf33-5107-9dec-e063-6294a90a5fcd	2026-08-20	Warnings	Exact identifier unii: ETJ7Z6XBU4
Sweat Resistant Sunscreen Body Original	TITANIUM DIOXIDE, ZINC OXIDE	Clutch, Inc.	4bbde755-e312-123e-e063-6294a90a467f	2026-08-20	Warnings	Exact identifier unii: 15FIX9V2JP
Psorinum Complex	PHOSPHORUS, SILICEA, SULPHUR, ALOE	BioActive Nutritional, Inc.	d4746927-e6d4-463d-a084-56ffc48d1e67	2026-08-20	Warnings	Exact identifier unii: ETJ7Z6XBU4
Boneforce HP	CALCAREA CARBONICA, CALCAREA FLUORICA, CALCAREA PHOSPHORICA, HEKLA LAVA, HYDROFLUORICUM ACIDUM, RHUS TOX, SILICEA, SYMPHYTUM OFFICINALE	BioActive Nutritional, Inc.	d96ca52b-781d-431c-ad2a-a54fd57eb106	2026-08-20	Warnings	Exact identifier unii: ETJ7Z6XBU4
HEADHUNTER SURF SCREEN SPF 50 SUNSCREEN	ZINC OXIDE,TITANIUM DIOXIDE	Guangzhou Tata Biotechnology Co., Ltd.	4339df13-77d3-31a1-e063-6394a90a5208	2026-08-17	Warnings	Exact identifier unii: 15FIX9V2JP
Cerebellum Thalamus A Aurm	CEREBELLUM THALAMUS A AURUM	Uriel Pharmacy Inc.	e1c395b8-9221-401f-8980-c91ff8843458	2026-08-17	Warnings	Exact identifier unii: ETJ7Z6XBU4

Reported adverse events (FAERS/openFDA)#

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