NDC 51672-4033-01 - Warfarin Sodium

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: 51672-4033
Requested NDC: 51672-4033-01
Package NDCs from labels: 51672-4033-1, 51672-4033-3, 51672-4033-7, 51672-4033-0, 51672-4033-01
Manufacturer: Sun Pharmaceutical Industries, Inc. | Taro Pharmaceutical Industries Ltd.
Effective date: 2025-06-10
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Warfarin Sodium	Sun Pharmaceutical Industries, Inc. \| Taro Pharmaceutical Industries Ltd.	2025-06-10	HUMAN PRESCRIPTION DRUG LABEL
Warfarin Sodium - Med-Health Pharma, LLC	Med-Health Pharma, LLC	2012-01-20	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
51672-4033-0	Warfarin Sodium	10 in 1 BLISTER PACK	TABLET	10	14
51672-4033-0	Warfarin Sodium	10 in 1 CARTON	TABLET	10	14
51672-4033-1	Warfarin Sodium	100 in 1 BOTTLE	TABLET	100	14
51672-4033-3	Warfarin Sodium	1000 in 1 BOTTLE	TABLET	1000	14
51672-4033-7	Warfarin Sodium	5000 in 1 BOTTLE	TABLET	5000	14

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
51672-4033	WARFARIN SODIUM TABLET [TARO PHARMACEUTICALS U.S.A., INC.]	13	Current NDC, Legacy NDC, 5 package rows	20231222_8ad881e0-ca41-42ad-9d7d-eb85b3a30af0.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
51672-4033-1	EA - Each	51672-4033	961cae87-3df2-47c4-9726-49436f1de469	1	2012-07-24
51672-4033-3	EA - Each	51672-4033	46e78dcb-7244-4f3e-be03-0dc10ac852a6	1	2012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
Warfarin Sodium	ACTIVE INGREDIENT	6153CWM0CL	WARFARIN SODIUM TABLET [TARO PHARMACEUTICALS U.S.A., INC.]	3
Warfarin	ACTIVE MOIETY	5Q7ZVV76EI	WARFARIN SODIUM TABLET [TARO PHARMACEUTICALS U.S.A., INC.]	3
Aluminum Oxide	INACTIVE INGREDIENT	LMI26O6933	WARFARIN SODIUM TABLET [TARO PHARMACEUTICALS U.S.A., INC.]	3
anhydrous lactose	INACTIVE INGREDIENT	3SY5LH9PMK	WARFARIN SODIUM TABLET [TARO PHARMACEUTICALS U.S.A., INC.]	3
Barium Oxide	INACTIVE INGREDIENT	77603K202B	WARFARIN SODIUM TABLET [TARO PHARMACEUTICALS U.S.A., INC.]	3
D&C Red No. 6	INACTIVE INGREDIENT	481744AI4O	WARFARIN SODIUM TABLET [TARO PHARMACEUTICALS U.S.A., INC.]	3
D&C Yellow No. 10	INACTIVE INGREDIENT	35SW5USQ3G	WARFARIN SODIUM TABLET [TARO PHARMACEUTICALS U.S.A., INC.]	3
FD&C Blue No. 1	INACTIVE INGREDIENT	H3R47K3TBD	WARFARIN SODIUM TABLET [TARO PHARMACEUTICALS U.S.A., INC.]	3
FD&C Blue No. 2	INACTIVE INGREDIENT	L06K8R7DQK	WARFARIN SODIUM TABLET [TARO PHARMACEUTICALS U.S.A., INC.]	3
FD&C Red No. 40	INACTIVE INGREDIENT	WZB9127XOA	WARFARIN SODIUM TABLET [TARO PHARMACEUTICALS U.S.A., INC.]	3
magnesium stearate	INACTIVE INGREDIENT	70097M6I30	WARFARIN SODIUM TABLET [TARO PHARMACEUTICALS U.S.A., INC.]	3
starch, corn	INACTIVE INGREDIENT	O8232NY3SJ	WARFARIN SODIUM TABLET [TARO PHARMACEUTICALS U.S.A., INC.]	3
Warfarin Sodium	ACTIVE INGREDIENT	6153CWM0CL	WARFARIN SODIUM TABLET [MED-HEALTH PHARMA, LLC]	2
Warfarin	ACTIVE MOIETY	5Q7ZVV76EI	WARFARIN SODIUM TABLET [MED-HEALTH PHARMA, LLC]	2
Aluminum Oxide	INACTIVE INGREDIENT	LMI26O6933	WARFARIN SODIUM TABLET [MED-HEALTH PHARMA, LLC]	2
anhydrous lactose	INACTIVE INGREDIENT	3SY5LH9PMK	WARFARIN SODIUM TABLET [MED-HEALTH PHARMA, LLC]	2
Barium Oxide	INACTIVE INGREDIENT	77603K202B	WARFARIN SODIUM TABLET [MED-HEALTH PHARMA, LLC]	2
D&C Red No. 6	INACTIVE INGREDIENT	481744AI4O	WARFARIN SODIUM TABLET [MED-HEALTH PHARMA, LLC]	2
D&C Yellow No. 10	INACTIVE INGREDIENT	35SW5USQ3G	WARFARIN SODIUM TABLET [MED-HEALTH PHARMA, LLC]	2
FD&C Blue No. 1	INACTIVE INGREDIENT	H3R47K3TBD	WARFARIN SODIUM TABLET [MED-HEALTH PHARMA, LLC]	2
FD&C Blue No. 2	INACTIVE INGREDIENT	L06K8R7DQK	WARFARIN SODIUM TABLET [MED-HEALTH PHARMA, LLC]	2
FD&C Red No. 40	INACTIVE INGREDIENT	WZB9127XOA	WARFARIN SODIUM TABLET [MED-HEALTH PHARMA, LLC]	2
magnesium stearate	INACTIVE INGREDIENT	70097M6I30	WARFARIN SODIUM TABLET [MED-HEALTH PHARMA, LLC]	2
starch, corn	INACTIVE INGREDIENT	O8232NY3SJ	WARFARIN SODIUM TABLET [MED-HEALTH PHARMA, 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 · 164 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Warfarin Sodium	WARFARIN SODIUM	Proficient Rx LP	73048ed9-242f-4f86-a8db-9c7547daa01d	2020-05-01	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 855296 rxcui: 855312 unii: 6153CWM0CL
H.M.D.	ALLIUM SAT, AVENA, BERBER VULG, LAPPA, PHYTOLACCA, SOLIDAGO, ALUMINA, ARG NIT, BARYTA CARB, BERYLLIUM, CADMIUM MET, CURPRUM MET, FLUORICUM ACIDUM, INDIUM, IODIUM, LITHIUM CARB, MERC SOLUB, NICCOLUM CARB, NITROGENUM OXYGENATUM, PLUMB MET, SELENIUM, STRONTIUM CARB, TITANIUM, ARSENICUM ALB, NAT MUR, NUX VOM	Zorex International	8c53091a-904d-4756-93e4-17143c5b48e9	2018-12-21	Warnings	Exact identifier unii: LMI26O6933
Tox-Chord	ALFALFA, ALUMINA, BENZOICUM ACIDUM, CARBONEUM, CETRARIA ISLANDICA, FOLLICULINUM, FUCUS VESICULOSUS, FUMARICUM ACIDUM, HEPAR SUIS, KALI CARBONICUM, KREOSOTUM, NATRUM MURIATICUM, PARAFFINUM, PETROLEUM, PHOSPHORICUM ACIDUM, PHOSPHORUS, PIX LIQUIDA, PLANTAGO MAJOR, PLUMBUM METALLICUM, PULSATILLA (VULGARIS), RADIUM BROMATUM, RESORCINUM, SALOL, SILICEA, SYMPHYTUM OFFICINALE, TABACUM, TEREBINTHINA, THYROIDINUM (BOVINE), TRITICUM REPENS, ZINCUM OXYDATUM	Energetix Corp	6b0d1628-b20d-426e-9c84-5cceadca3f45	2016-11-11	Warnings	Exact identifier unii: LMI26O6933
e2447944-15e9-4074-aff0-2c90a7c04694			b1b766b1-0327-48cd-ab01-e85038cf365f	2012-01-20	Boxed warning, Warnings, Adverse reactions	Exact identifier spl id: e2447944-15e9-4074-aff0-2c90a7c04694 spl set id: b1b766b1-0327-48cd-ab01-e85038cf365f

Reported adverse events (FAERS/openFDA)#

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