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 4 of 133 · 2,643 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Leg Cramps PM	OYSTER SHELL CALCIUM CARBONATE, CRUDE, CAUSTICUM, MATRICARIA RECUTITA, CINCHONA OFFICINALIS BARK, COPPER, LYCOPODIUM CLAVATUM SPORE, MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE, TOXICODENDRON PUBESCENS LEAF, SILICON DIOXIDE, AND SULFUR	Hyland's Inc.	b0574a7e-88fa-417e-b6d5-60ced59eba47	2026-07-15	Warnings	Exact identifier unii: ETJ7Z6XBU4
Jacksons Cell Salts SILICA 12X 12	SILICEA	Zettl Health Inc.	5647dafc-1fff-6a25-e063-6294a90a8b4f	2026-07-10		Exact identifier unii: ETJ7Z6XBU4
Bombee Honey Daily Glow Shield Sunscreen	HOMOSALATE, OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE	ABT ASIA Inc.	56112dff-b091-7a56-e063-6294a90a77d3	2026-07-08	Warnings	Exact identifier unii: 15FIX9V2JP
Stay Ageless Tinted Mineral Sunscreen	BROAD SPECTRUM SPF30	DERMIO DERMATOLOGY LLC	562f5b0d-6a10-305d-e063-6394a90a5980	2026-07-08	Warnings	Exact identifier unii: 15FIX9V2JP
Stay Ageless Tinted Mineral Sunscreen	BROAD SPECTRUM SPF30	Suzanne's Skin2soul LLC	562fbaa6-f93a-5ec4-e063-6294a90a9634	2026-07-08	Warnings	Exact identifier unii: 15FIX9V2JP
Aussie Betta Tallow Sunscreen SPF50 SPF50	TITANIUM DIOXIDE AND ZINC OXIDE SUNSCREEN	AUSSIE BETTA HEALTHY CARE PTY LTD	56007d82-ff5b-6c26-e063-6294a90a09b6	2026-07-07	Warnings	Exact identifier unii: 15FIX9V2JP
Artificial Tears	ARTIFICIAL TEARS	AvPAK	f18bebf2-1936-658f-e053-2a95a90a5012	2026-07-07	Warnings	Exact identifier unii: 3NXW29V3WO
EELHOE Body Coverage Perfector	TITANIUM DIOXIDE	Shantou Eelhoe Daily Chemical Technology Co., Ltd.	5610c3b7-456b-3bc1-e063-6394a90a3fa8	2026-07-07	Warnings	Exact identifier unii: 15FIX9V2JP
Premier Tinted Mineral Sunscreen	BROAD SPECTRUM SPF30	Emerald Aesthetics LLC	55f88dd1-346c-22a5-e063-6294a90a711f	2026-07-06	Warnings	Exact identifier unii: 15FIX9V2JP
OHUI Ultimate Cover CC Cushion Compact 02 Natural Beige	TITANIUM DIOXIDE	LG H&H Co., Ltd.	d307471c-6cc6-ce48-e053-2995a90a3e02	2026-07-02	Warnings	Exact identifier unii: 15FIX9V2JP
Evereden Fluid Silk Mineral Sunscreen PRO SPF50	TITANIUM DIOXIDE, ZINC OXIDE	Eden Brands Inc.	2cb7773f-9a05-ad02-e063-6294a90af024	2026-07-01	Warnings	Exact identifier unii: 15FIX9V2JP
The Cell Salt Co. Daily Blend 12 in 1	CALC FLUOR, CALC PHOS, CALC SULPH, FERRUM PHOS, KALI MUR, KALI PHOS, KALI SULPH, MAG PHOS, NAT MUR, NAT PHOS, NAT SULPH, SILICEA	The Cell Salt Company LLC	55826f59-acf4-7370-e063-6394a90afed7	2026-07-01	Warnings	Exact identifier unii: ETJ7Z6XBU4
OHUI Ultimate Cover CC Cushion Compact 01 Light Beige	TITANIUM DIOXIDE	LG H&H Co., Ltd.	d2f9c54b-ac4e-5141-e053-2a95a90aa2b8	2026-06-30	Warnings	Exact identifier unii: 15FIX9V2JP
Bambusa Stannum	BAMBUSA STANNUM	Uriel Pharmacy Inc.	a0d4d0ac-e2d2-4381-8f93-e41719521859	2026-06-30	Warnings	Exact identifier unii: ETJ7Z6XBU4
TOCOBO Blur Finish Sun Cushion Cotton Blue	HOMOSALATE, OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDE	PICTON Co., Ltd.	4d6ddee3-9a76-6c9c-e063-6394a90a1529	2026-06-29	Warnings	Exact identifier unii: 15FIX9V2JP
Earth Baby Broad Spectrum SPF 30	SUNSCREEN	Earth Baby, Inc.	42556876-74ea-38e6-e054-00144ff8d46c	2026-06-28	Warnings	Exact identifier unii: 15FIX9V2JP
Sun Does Matter Daily Face Sunscreen	HOMOSALATE, OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE	Sundoesmatter Company Inc.	553687d8-d4e1-8361-e063-6294a90a24fe	2026-06-27	Warnings	Exact identifier unii: 15FIX9V2JP
Ivory Perfecting Makeup Broad Spectrum SPF 25	OCTINOXATE, TITANIUM DIOXIDE	Merle Norman Cosmetics, Inc	552f25ba-61d5-6a94-e063-6394a90a46e9	2026-06-26	Warnings	Exact identifier unii: 15FIX9V2JP
Simply Beige Perfecting Makeup Broad Spectrum SPF 25	OCTINOXATE, TITANIUM DIOXIDE	Merle Norman Cosmetics, Inc	552f4799-9122-8db5-e063-6394a90a5132	2026-06-26	Warnings	Exact identifier unii: 15FIX9V2JP
Vanilla Perfecting Makeup Broad Spectrum SPF 25	OCTINOXATE, TITANIUM DIOXIDE	Merle Norman Cosmetics, Inc	552f6d2c-9b8c-aa52-e063-6294a90a787e	2026-06-26	Warnings	Exact identifier unii: 15FIX9V2JP

Reported adverse events (FAERS/openFDA)#

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