NDC 0832-1218-89 - Jantoven

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: 0832-1218
Requested NDC: 0832-1218-89
Package NDCs from labels: 0832-1218-00, 0832-1218-50, 0832-1218-89, 0832-1218-01
Manufacturer: Upsher-Smith Laboratories, LLC | Bora Pharmaceuticals, Inc
Effective date: 2025-07-08
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Jantoven - Upsher-Smith Laboratories, LLC \| Bora Pharmaceuticals, Inc	Upsher-Smith Laboratories, LLC \| Bora Pharmaceuticals, Inc	2025-07-08	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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
0832-1218-00	Jantoven	100 in 1 BOTTLE	TABLET	100	13
0832-1218-01	Jantoven	100 in 1 CARTON	TABLET	100	13
0832-1218-50	Jantoven	500 in 1 BOTTLE	TABLET	500	13
0832-1218-89	Jantoven	1 in 1 BLISTER PACK	TABLET	1	13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0832-1218	JANTOVEN (WARFARIN SODIUM) TABLET [UPSHER-SMITH LABORATORIES, LLC]	12	Current NDC, Legacy NDC, 4 package rows	20230413_19a69a72-ac5d-45d5-a94d-a5aaecbe4730.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
0832-1218-00	EA - Each	0832-1218	4f75a7af-c1b9-4c44-9d39-261c64b4890d	1	2012-07-24
0832-1218-01	EA - Each	0832-1218	dacef602-c55b-4cbe-be36-d51196c18958	1	2012-07-24
0832-1218-50	EA - Each	0832-1218	507f05c8-30f0-4fae-8571-4506e3cf8406	1	2012-07-24
0832-1218-89	EA - Each	0832-1218	2b818c29-8420-47b1-9e18-5fb7360515bd	1	2012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
Warfarin Sodium	ACTIVE INGREDIENT	6153CWM0CL	JANTOVEN (WARFARIN SODIUM) TABLET [UPSHER-SMITH LABORATORIES, INC.]	7
Warfarin	ACTIVE MOIETY	5Q7ZVV76EI	JANTOVEN (WARFARIN SODIUM) TABLET [UPSHER-SMITH LABORATORIES, INC.]	7
Brown Iron Oxide	INACTIVE INGREDIENT	1N032N7MFO	JANTOVEN (WARFARIN SODIUM) TABLET [UPSHER-SMITH LABORATORIES, INC.]	7
D&C YELLOW NO. 10	INACTIVE INGREDIENT	35SW5USQ3G	JANTOVEN (WARFARIN SODIUM) TABLET [UPSHER-SMITH LABORATORIES, INC.]	7
FD&C BLUE NO. 1	INACTIVE INGREDIENT	H3R47K3TBD	JANTOVEN (WARFARIN SODIUM) TABLET [UPSHER-SMITH LABORATORIES, INC.]	7
FD&C BLUE NO. 2	INACTIVE INGREDIENT	L06K8R7DQK	JANTOVEN (WARFARIN SODIUM) TABLET [UPSHER-SMITH LABORATORIES, INC.]	7
FD&C RED NO. 40	INACTIVE INGREDIENT	WZB9127XOA	JANTOVEN (WARFARIN SODIUM) TABLET [UPSHER-SMITH LABORATORIES, INC.]	7
FD&C YELLOW NO. 6	INACTIVE INGREDIENT	H77VEI93A8	JANTOVEN (WARFARIN SODIUM) TABLET [UPSHER-SMITH LABORATORIES, INC.]	7
FERRIC OXIDE YELLOW	INACTIVE INGREDIENT	EX438O2MRT	JANTOVEN (WARFARIN SODIUM) TABLET [UPSHER-SMITH LABORATORIES, INC.]	7
FERROSOFERRIC OXIDE	INACTIVE INGREDIENT	XM0M87F357	JANTOVEN (WARFARIN SODIUM) TABLET [UPSHER-SMITH LABORATORIES, INC.]	7
lactose monohydrate	INACTIVE INGREDIENT	EWQ57Q8I5X	JANTOVEN (WARFARIN SODIUM) TABLET [UPSHER-SMITH LABORATORIES, INC.]	7
magnesium stearate	INACTIVE INGREDIENT	70097M6I30	JANTOVEN (WARFARIN SODIUM) TABLET [UPSHER-SMITH LABORATORIES, INC.]	7
povidones	INACTIVE INGREDIENT	FZ989GH94E	JANTOVEN (WARFARIN SODIUM) TABLET [UPSHER-SMITH LABORATORIES, INC.]	7
starch, corn	INACTIVE INGREDIENT	O8232NY3SJ	JANTOVEN (WARFARIN SODIUM) TABLET [UPSHER-SMITH LABORATORIES, INC.]	7

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 8 · 144 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Warfarin Sodium	WARFARIN	Aphena Pharma Solutions - Tennessee, LLC	a98916a5-cdb2-4251-bdea-0245c763b2f1	2020-12-15	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 855324 rxcui: 855312 unii: 6153CWM0CL
Warfarin Sodium	WARFARIN	Exelan Pharmaceuticals Inc.	c0cc4511-e656-4b6d-96cd-e02e76173b9d	2020-09-09	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 855324 rxcui: 855296 rxcui: 855344 rxcui: 855302 rxcui: 855288 rxcui: 855338 rxcui: 855318 rxcui: 855312 rxcui: 855332 unii: 6153CWM0CL
Warfarin Sodium	WARFARIN	Aphena Pharma Solutions - Tennessee, LLC	91f24482-d4cb-4a09-a97e-64f6e49071ee	2020-08-03	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 855332 unii: 6153CWM0CL
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

Reported adverse events (FAERS/openFDA)#

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