NDC 68084-348-11 - Losartan Potassium

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: 68084-348
Requested NDC: 68084-348-11
Package NDCs from labels: 68084-348-11, 68084-348-01
Manufacturer: Cardinal Health 107, LLC
Effective date: 2026-08-27
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Losartan Potassium - Cardinal Health 107, LLC	Cardinal Health 107, LLC	2026-08-27	HUMAN PRESCRIPTION DRUG LABEL
Losartan Potassium - American Health Packaging	American Health Packaging	2026-06-24	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	Strength	SPL version
68084-348-01	Losartan Potassium	100 in 1 BOX, UNIT-DOSE	TABLET, FILM COATED	100		9
68084-348-11	Losartan Potassium	1 in 1 BLISTER PACK	TABLET, FILM COATED	1		9

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
68084-348	LOSARTAN POTASSIUM TABLET, FILM COATED [AMERICAN HEALTH PACKAGING]	9	Current NDC, Legacy NDC, 2 package rows	20241010_e7f6b25b-ec4c-4c3a-a541-617d2d9ab393.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
68084-348-01	EA - Each	68084-348	8e0fb305-225b-40ed-89a5-c873d66dc218	1	2012-07-24
68084-348-11	EA - Each	68084-348	946d3019-014d-47fe-9cd8-8efe27a9b767	1	2012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
LOSARTAN POTASSIUM	ACTIVE INGREDIENT	3ST302B24A	LOSORTAN POTASSIUM (LOSARTAN POTASSIUM) TABLET, FILM COATED [CARDINAL HEALTH]	8
LOSARTAN	ACTIVE MOIETY	JMS50MPO89	LOSORTAN POTASSIUM (LOSARTAN POTASSIUM) TABLET, FILM COATED [CARDINAL HEALTH]	8
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	LOSORTAN POTASSIUM (LOSARTAN POTASSIUM) TABLET, FILM COATED [CARDINAL HEALTH]	8
HYDROXYPROPYL CELLULOSE, LOW SUBSTITUTED	INACTIVE INGREDIENT	2165RE0K14	LOSORTAN POTASSIUM (LOSARTAN POTASSIUM) TABLET, FILM COATED [CARDINAL HEALTH]	8
HYPROMELLOSES	INACTIVE INGREDIENT	3NXW29V3WO	LOSORTAN POTASSIUM (LOSARTAN POTASSIUM) TABLET, FILM COATED [CARDINAL HEALTH]	8
LACTOSE MONOHYDRATE	INACTIVE INGREDIENT	EWQ57Q8I5X	LOSORTAN POTASSIUM (LOSARTAN POTASSIUM) TABLET, FILM COATED [CARDINAL HEALTH]	8
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	LOSORTAN POTASSIUM (LOSARTAN POTASSIUM) TABLET, FILM COATED [CARDINAL HEALTH]	8
POLYETHYLENE GLYCOLS	INACTIVE INGREDIENT	3WJQ0SDW1A	LOSORTAN POTASSIUM (LOSARTAN POTASSIUM) TABLET, FILM COATED [CARDINAL HEALTH]	8
SILICON DIOXIDE	INACTIVE INGREDIENT	ETJ7Z6XBU4	LOSORTAN POTASSIUM (LOSARTAN POTASSIUM) TABLET, FILM COATED [CARDINAL HEALTH]	8
SODIUM STARCH GLYCOLATE TYPE A POTATO	INACTIVE INGREDIENT	5856J3G2A2	LOSORTAN POTASSIUM (LOSARTAN POTASSIUM) TABLET, FILM COATED [CARDINAL HEALTH]	8
STARCH, CORN	INACTIVE INGREDIENT	O8232NY3SJ	LOSORTAN POTASSIUM (LOSARTAN POTASSIUM) TABLET, FILM COATED [CARDINAL HEALTH]	8
TALC	INACTIVE INGREDIENT	7SEV7J4R1U	LOSORTAN POTASSIUM (LOSARTAN POTASSIUM) TABLET, FILM COATED [CARDINAL HEALTH]	8
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	LOSORTAN POTASSIUM (LOSARTAN POTASSIUM) TABLET, FILM COATED [CARDINAL HEALTH]	8
LOSARTAN POTASSIUM	ACTIVE INGREDIENT	3ST302B24A	LOSORTAN POTASSIUM (LOSARTAN POTASSIUM) TABLET, FILM COATED [AMERICAN HEALTH PACKAGING]	3
LOSARTAN	ACTIVE MOIETY	JMS50MPO89	LOSORTAN POTASSIUM (LOSARTAN POTASSIUM) TABLET, FILM COATED [AMERICAN HEALTH PACKAGING]	3
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	LOSORTAN POTASSIUM (LOSARTAN POTASSIUM) TABLET, FILM COATED [AMERICAN HEALTH PACKAGING]	3
HYDROXYPROPYL CELLULOSE, LOW SUBSTITUTED	INACTIVE INGREDIENT	2165RE0K14	LOSORTAN POTASSIUM (LOSARTAN POTASSIUM) TABLET, FILM COATED [AMERICAN HEALTH PACKAGING]	3
HYPROMELLOSES	INACTIVE INGREDIENT	3NXW29V3WO	LOSORTAN POTASSIUM (LOSARTAN POTASSIUM) TABLET, FILM COATED [AMERICAN HEALTH PACKAGING]	3
LACTOSE MONOHYDRATE	INACTIVE INGREDIENT	EWQ57Q8I5X	LOSORTAN POTASSIUM (LOSARTAN POTASSIUM) TABLET, FILM COATED [AMERICAN HEALTH PACKAGING]	3
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	LOSORTAN POTASSIUM (LOSARTAN POTASSIUM) TABLET, FILM COATED [AMERICAN HEALTH PACKAGING]	3
POLYETHYLENE GLYCOLS	INACTIVE INGREDIENT	3WJQ0SDW1A	LOSORTAN POTASSIUM (LOSARTAN POTASSIUM) TABLET, FILM COATED [AMERICAN HEALTH PACKAGING]	3
SILICON DIOXIDE	INACTIVE INGREDIENT	ETJ7Z6XBU4	LOSORTAN POTASSIUM (LOSARTAN POTASSIUM) TABLET, FILM COATED [AMERICAN HEALTH PACKAGING]	3
SODIUM STARCH GLYCOLATE TYPE A POTATO	INACTIVE INGREDIENT	5856J3G2A2	LOSORTAN POTASSIUM (LOSARTAN POTASSIUM) TABLET, FILM COATED [AMERICAN HEALTH PACKAGING]	3
STARCH, CORN	INACTIVE INGREDIENT	O8232NY3SJ	LOSORTAN POTASSIUM (LOSARTAN POTASSIUM) TABLET, FILM COATED [AMERICAN HEALTH PACKAGING]	3
TALC	INACTIVE INGREDIENT	7SEV7J4R1U	LOSORTAN POTASSIUM (LOSARTAN POTASSIUM) TABLET, FILM COATED [AMERICAN HEALTH PACKAGING]	3
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	LOSORTAN POTASSIUM (LOSARTAN POTASSIUM) TABLET, FILM COATED [AMERICAN HEALTH PACKAGING]	3

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 71 of 140 · 2,789 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
DENTI BUONGIORNO PLAQUE CARE TOOTH	SILICA, SODIUM FLUORIDE, TOCOPHERYL ACETATE, TETRASODIUM PYROPHOSPHATE	DONG IL PHARMS CO.,LTD	41157552-2473-176b-e063-6294a90a9ad0	2025-10-13	Warnings	Exact identifier unii: ETJ7Z6XBU4
DENTI BUONGIORNO GUM CARE TOOTH	SILICA, SODIUM FLUORIDE, TOCOPHERYL ACETATE	ATOSAFE CO., Ltd	4115d122-3090-d3e5-e063-6294a90aafb6	2025-10-13	Warnings	Exact identifier unii: ETJ7Z6XBU4
DENTI BUONGIORNO GUM CARE TOOTH	SILICA, SODIUM FLUORIDE, TOCOPHERYL ACETATE	DONG IL PHARMS CO.,LTD	4115b653-63ff-703f-e063-6294a90a652a	2025-10-13	Warnings	Exact identifier unii: ETJ7Z6XBU4
Losartan Potassium	LOSARTAN POTASSIUM	NorthStar RxLLC	394398e1-119e-4943-b414-27261f5d4842	2025-10-10	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 979480 rxcui: 979492 rxcui: 979485 unii: 3ST302B24A
Vertra S Dorian Kona Gold Signature Face Stick SPF 38	TITANIUM DIOXIDE	Eai-jr 286, Inc	b6c316c3-661b-6428-e053-2a95a90a1a6b	2025-10-10	Warnings	Exact identifier unii: 15FIX9V2JP
Silicea Belladonna	SILICEA BELLADONNA	Uriel Pharmacy Inc.	a142eb87-c5fb-4138-bc98-e7f1391fe221	2025-10-10	Warnings	Exact identifier unii: ETJ7Z6XBU4
Losartan Potassium	LOSARTAN POTASSIUM	Camber Pharmaceuticals, Inc.	cafd54e8-42a8-474c-8ea8-49ec74c2b0d3	2025-10-09	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 979480 rxcui: 979492 rxcui: 979485 unii: 3ST302B24A
Dr Lift Mineral SPF 50	TITANIUM DIOXIDE, ZINC OXIDE	Spa de Soleil	40c03d65-8d09-371a-e063-6294a90a7ac6	2025-10-09	Warnings	Exact identifier unii: 15FIX9V2JP
Dr Lift Mineral SPF 30	TITANIUM DIOXIDE	Spa de Soleil	40c0e0d2-2c1d-e629-e063-6394a90a5aaf	2025-10-09	Warnings	Exact identifier unii: 15FIX9V2JP
Essential Defense Mineral Shield Broad Spectrum SPF 35 Sunscreen	TITANIUM DIOXIDE AND ZINC OXIDE	Allergan, Inc.	29817fdc-f14c-4013-a8ed-4367f3b2867c	2025-10-09	Warnings	Exact identifier unii: 15FIX9V2JP
Losartan Potassium	LOSARTAN POTASSIUM	Alembic Pharmaceuticals Limited	eeb77c84-38d3-432d-914a-54b312b374bd	2025-10-08	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 979480 rxcui: 979492 rxcui: 979485 unii: 3ST302B24A
Vertra Pearl White Face Stick SPF 50	PADIMATE O, TITANIUM DIOXIDE	Eai-jr 286, Inc	b69a75e0-8724-35ae-e053-2a95a90a5f34	2025-10-07	Warnings	Exact identifier unii: 15FIX9V2JP
Vertra Mick Fanning Signature Foundation Sunscreen Face Stick SPF 35 Coolangatta Beige	TITANIUM DIOXIDE	EAI-JR 286, Inc.	b9ea12e8-6ed9-d805-e053-2a95a90aa107	2025-10-07	Warnings	Exact identifier unii: 15FIX9V2JP
SPF50 Sunscreen	SUNSCREEN	KINGKEY MBC LIFE TECHNOLOGY GROUP CO., LTD	b3cde609-7d62-2ac7-e053-2a95a90a26b3	2025-10-07		Exact identifier unii: 15FIX9V2JP
Parathyropar	SYMPHYTUM OFFICINALE, BARYTA CARBONICA, CALCAREA CARBONICA, CALCAREA PHOSPHORICA, HEKLA LAVA, MANGANUM METALLICUM, RHUS TOX, SILICEA, PARATHORMONUM	Energique, Inc.	bd13617a-c470-4421-8f47-43a98036f40b	2025-10-06	Warnings	Exact identifier unii: ETJ7Z6XBU4
Mitochondria PRO	ARALIA QUINQUEFOLIA, ARNICA MONTANA, ADENOSINUM TRIPHOSPHORICUM DINATRUM, ALPHA-KETOGLUTARICUM ACIDUM, ASCORBICUM ACIDUM, ALPHA-LIPOICUM ACIDUM, CALCAREA CARBONICA, CITRICUM ACIDUM, CUPRUM METALLICUM, CYSTEINUM, FERRUM METALLICUM, IODIUM, LEVOTHYROXINUM, MAGNESIUM GLUCONICUM DIHYDRICUM, MALICUM ACIDUM, MANGANUM ACETICUM, NADIDUM, NATRUM PYRUVICUM, NICOTINAMIDUM, PYRIDOXINUM HYDROCHLORICUM, RIBOFLAVINUM, SELENIUM METALLICUM, SULPHUR, THIAMINUM HYDROCHLORICUM, UBIDECARENONUM, ZINCUM METALLICUM,	Energique, Inc.	8c3e961d-bc33-40cd-a282-a4fe5aa3f0ad	2025-10-06	Warnings	Exact identifier unii: ETJ7Z6XBU4
Vertra Mick Fanning Signature Foundation Sunscreen Face Stick SPF 35 Coolangatta Beige	TITANIUM DIOXIDE	Toshiki Pigment Co., Ltd.	b9eba15f-493a-43c9-e053-2995a90a0451	2025-10-06	Warnings	Exact identifier unii: 15FIX9V2JP
Tri-Relief Antifungal	SODIUM CHLORIDE, SILICON DIOXIDE, AND THUJA OCCIDENTALIS LEAFY TWIG	Forces of Nature	6fe97b54-8aa3-4d86-9055-0629589a416b	2025-10-06	Warnings	Exact identifier unii: ETJ7Z6XBU4
PURE SOL SPF 37 Tinted Moisturizer	ZINC OXIDE TITANIUM DIOXIDE	Brand 2022b LLC	4052c4e4-2105-80c0-e063-6294a90af41d	2025-10-04	Warnings	Exact identifier unii: 15FIX9V2JP
ARBLI	LOSARTAN POTASSIUM	Scienture LLC	afd2d1ba-e7af-4e4e-8b7e-a9f72612fc97	2025-10-03	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: 3ST302B24A

Reported adverse events (FAERS/openFDA)#

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