NDC 51672-4026-01 - Ketoconazole

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: 51672-4026
Requested NDC: 51672-4026-01
Package NDCs from labels: 51672-4026-6, 51672-4026-1, 51672-4026-2, 51672-4026-8, 51672-4026-9, 51672-4026-0, 51672-4026-01
Manufacturer: Bryant Ranch Prepack
Effective date: 2025-11-18
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Ketoconazole - Bryant Ranch Prepack	Bryant Ranch Prepack	2025-11-18	HUMAN PRESCRIPTION DRUG LABEL
Ketoconazole Tablets USP, 200 mg	Golden State Medical Supply, Inc.	2025-11-17	HUMAN PRESCRIPTION DRUG LABEL
Ketoconazole Tablets USP, 200 mg	Sun Pharmaceutical Industries, Inc. \| Taro Pharmaceutical Industries Ltd.	2025-09-02	HUMAN PRESCRIPTION DRUG LABEL
Ketoconazole - Direct_Rx	Direct_Rx	2025-01-22	HUMAN PRESCRIPTION DRUG LABEL
Ketoconazole Tablets USP, 200 mg	REMEDYREPACK INC.	2024-06-04	HUMAN PRESCRIPTION DRUG LABEL
Ketoconazole Tablets USP, 200 MG	NuCare Pharmaceuticals,Inc.	2022-12-13	HUMAN PRESCRIPTION DRUG LABEL
Ketoconazole Tablets USP, 200 MG	PD-Rx Pharmaceuticals, Inc.	2021-12-09	HUMAN PRESCRIPTION DRUG LABEL
Ketoconazole Tablets USP, 200 MG	Preferred Pharmaceuticals, Inc.	2020-06-19	HUMAN PRESCRIPTION DRUG LABEL
Ketoconazole Tablets USP, 200 MG	NuCare Pharmaceuticals, Inc.	2017-07-24	HUMAN PRESCRIPTION DRUG LABEL
Ketoconazole - Aidarex Pharmaceuticals LLC	Aidarex Pharmaceuticals LLC	2014-01-05	HUMAN PRESCRIPTION DRUG LABEL
Ketoconazole - Physicians Total Care, Inc.	Physicians Total Care, Inc.	2011-03-10	HUMAN PRESCRIPTION DRUG LABEL
Ketoconazole - Rebel Distributors Corp	Rebel Distributors Corp	2010-09-29	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
51672-4026-0	Ketoconazole	10 in 1 BLISTER PACK	TABLET	10	12
51672-4026-0	Ketoconazole	10 in 1 BOX	TABLET	10	12
51672-4026-1	Ketoconazole	100 in 1 BOTTLE	TABLET	100	12
51672-4026-2	Ketoconazole	500 in 1 BOTTLE	TABLET	500	12
51672-4026-6	Ketoconazole	30 in 1 BOTTLE	TABLET	30	12
51672-4026-8	Ketoconazole	3 in 1 BOX	TABLET	3	12
51672-4026-8	Ketoconazole	10 in 1 BLISTER PACK	TABLET	10	12
51672-4026-9	Ketoconazole	10 in 1 BLISTER PACK	TABLET	10	12
51672-4026-9	Ketoconazole	5 in 1 BOX	TABLET	5	12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
51672-4026	KETOCONAZOLE TABLET [TARO PHARMACEUTICALS U.S.A., INC.]	11	Current NDC, Legacy NDC, 9 package rows	20240524_8ca815a8-bccb-4ee2-a042-922373329cae.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
51672-4026-1	EA - Each	51672-4026	a53b7fa1-98a3-49e6-9f13-07af603854d6	1	2012-07-24
51672-4026-6	EA - Each	51672-4026	12e5aaf9-13ce-432d-9378-bfee61a1e11f	1	2012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
Ketoconazole	ACTIVE INGREDIENT	R9400W927I	KETOCONAZOLE TABLET [TARO PHARMACEUTICALS U.S.A., INC.]	5
Ketoconazole	ACTIVE MOIETY	R9400W927I	KETOCONAZOLE TABLET [TARO PHARMACEUTICALS U.S.A., INC.]	5
cellulose, microcrystalline	INACTIVE INGREDIENT	OP1R32D61U	KETOCONAZOLE TABLET [TARO PHARMACEUTICALS U.S.A., INC.]	5
lactose monohydrate	INACTIVE INGREDIENT	EWQ57Q8I5X	KETOCONAZOLE TABLET [TARO PHARMACEUTICALS U.S.A., INC.]	5
magnesium stearate	INACTIVE INGREDIENT	70097M6I30	KETOCONAZOLE TABLET [TARO PHARMACEUTICALS U.S.A., INC.]	5
povidones	INACTIVE INGREDIENT	FZ989GH94E	KETOCONAZOLE TABLET [TARO PHARMACEUTICALS U.S.A., INC.]	5
silicon dioxide	INACTIVE INGREDIENT	ETJ7Z6XBU4	KETOCONAZOLE TABLET [TARO PHARMACEUTICALS U.S.A., INC.]	5
starch, corn	INACTIVE INGREDIENT	O8232NY3SJ	KETOCONAZOLE TABLET [TARO PHARMACEUTICALS U.S.A., INC.]	5
Ketoconazole	ACTIVE INGREDIENT	R9400W927I	KETOCONAZOLE TABLET [GOLDEN STATE MEDICAL SUPPLY, INC.]	4
Ketoconazole	ACTIVE MOIETY	R9400W927I	KETOCONAZOLE TABLET [GOLDEN STATE MEDICAL SUPPLY, INC.]	4
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	KETOCONAZOLE TABLET [GOLDEN STATE MEDICAL SUPPLY, INC.]	4
colloidal silicon dioxide	INACTIVE INGREDIENT	ETJ7Z6XBU4	KETOCONAZOLE TABLET [GOLDEN STATE MEDICAL SUPPLY, INC.]	4
lactose monohydrate	INACTIVE INGREDIENT	EWQ57Q8I5X	KETOCONAZOLE TABLET [GOLDEN STATE MEDICAL SUPPLY, INC.]	4
magnesium stearate	INACTIVE INGREDIENT	70097M6I30	KETOCONAZOLE TABLET [GOLDEN STATE MEDICAL SUPPLY, INC.]	4
povidone	INACTIVE INGREDIENT	FZ989GH94E	KETOCONAZOLE TABLET [GOLDEN STATE MEDICAL SUPPLY, INC.]	4
STARCH, CORN	INACTIVE INGREDIENT	O8232NY3SJ	KETOCONAZOLE TABLET [GOLDEN STATE MEDICAL SUPPLY, INC.]	4
Ketoconazole	ACTIVE INGREDIENT	R9400W927I	KETOCONAZOLE TABLET [PREFERRED PHARMACEUTICALS, INC.]	2
Ketoconazole	ACTIVE MOIETY	R9400W927I	KETOCONAZOLE TABLET [PREFERRED PHARMACEUTICALS, INC.]	2
cellulose, microcrystalline	INACTIVE INGREDIENT	OP1R32D61U	KETOCONAZOLE TABLET [PREFERRED PHARMACEUTICALS, INC.]	2
lactose monohydrate	INACTIVE INGREDIENT	EWQ57Q8I5X	KETOCONAZOLE TABLET [PREFERRED PHARMACEUTICALS, INC.]	2
magnesium stearate	INACTIVE INGREDIENT	70097M6I30	KETOCONAZOLE TABLET [PREFERRED PHARMACEUTICALS, INC.]	2
povidones	INACTIVE INGREDIENT	FZ989GH94E	KETOCONAZOLE TABLET [PREFERRED PHARMACEUTICALS, INC.]	2
silicon dioxide	INACTIVE INGREDIENT	ETJ7Z6XBU4	KETOCONAZOLE TABLET [PREFERRED PHARMACEUTICALS, INC.]	2
starch, corn	INACTIVE INGREDIENT	O8232NY3SJ	KETOCONAZOLE TABLET [PREFERRED PHARMACEUTICALS, INC.]	2
KETOCONAZOLE	ACTIVE INGREDIENT	R9400W927I	KETOCONAZOLE TABLET [AIDAREX PHARMACEUTICALS LLC]	1
KETOCONAZOLE	ACTIVE INGREDIENT	R9400W927I	KETOCONAZOLE TABLET [PHYSICIANS TOTAL CARE, INC.]	1
Ketoconazole	ACTIVE INGREDIENT	R9400W927I	KETOCONAZOLE TABLET [REBEL DISTRIBUTORS CORP]	1
KETOCONAZOLE	ACTIVE MOIETY	R9400W927I	KETOCONAZOLE TABLET [AIDAREX PHARMACEUTICALS LLC]	1
KETOCONAZOLE	ACTIVE MOIETY	R9400W927I	KETOCONAZOLE TABLET [PHYSICIANS TOTAL CARE, INC.]	1
Ketoconazole	ACTIVE MOIETY	R9400W927I	KETOCONAZOLE TABLET [REBEL DISTRIBUTORS CORP]	1
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	KETOCONAZOLE TABLET [AIDAREX PHARMACEUTICALS LLC]	1
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	KETOCONAZOLE TABLET [PHYSICIANS TOTAL CARE, INC.]	1
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	KETOCONAZOLE TABLET [REBEL DISTRIBUTORS CORP]	1
lactose monohydrate	INACTIVE INGREDIENT	EWQ57Q8I5X	KETOCONAZOLE TABLET [REBEL DISTRIBUTORS CORP]	1
LACTOSE MONOHYDRATE	INACTIVE INGREDIENT	EWQ57Q8I5X	KETOCONAZOLE TABLET [AIDAREX PHARMACEUTICALS LLC]	1
LACTOSE MONOHYDRATE	INACTIVE INGREDIENT	EWQ57Q8I5X	KETOCONAZOLE TABLET [PHYSICIANS TOTAL CARE, INC.]	1
magnesium stearate	INACTIVE INGREDIENT	70097M6I30	KETOCONAZOLE TABLET [REBEL DISTRIBUTORS CORP]	1
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	KETOCONAZOLE TABLET [AIDAREX PHARMACEUTICALS LLC]	1
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	KETOCONAZOLE TABLET [PHYSICIANS TOTAL CARE, INC.]	1
POVIDONE	INACTIVE INGREDIENT	FZ989GH94E	KETOCONAZOLE TABLET [PHYSICIANS TOTAL CARE, INC.]	1
povidone	INACTIVE INGREDIENT	FZ989GH94E	KETOCONAZOLE TABLET [REBEL DISTRIBUTORS CORP]	1
POVIDONES	INACTIVE INGREDIENT	FZ989GH94E	KETOCONAZOLE TABLET [AIDAREX PHARMACEUTICALS LLC]	1
SILICON DIOXIDE	INACTIVE INGREDIENT	ETJ7Z6XBU4	KETOCONAZOLE TABLET [PHYSICIANS TOTAL CARE, INC.]	1
SILICON DIOXIDE	INACTIVE INGREDIENT	ETJ7Z6XBU4	KETOCONAZOLE TABLET [AIDAREX PHARMACEUTICALS LLC]	1
SILICON DIOXIDE	INACTIVE INGREDIENT	ETJ7Z6XBU4	KETOCONAZOLE TABLET [REBEL DISTRIBUTORS CORP]	1
STARCH, CORN	INACTIVE INGREDIENT	O8232NY3SJ	KETOCONAZOLE TABLET [PHYSICIANS TOTAL CARE, INC.]	1
STARCH, CORN	INACTIVE INGREDIENT	O8232NY3SJ	KETOCONAZOLE TABLET [REBEL DISTRIBUTORS CORP]	1
STARCH, CORN	INACTIVE INGREDIENT	O8232NY3SJ	KETOCONAZOLE TABLET [AIDAREX PHARMACEUTICALS LLC]	1

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 38 · 741 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
BioMicroneedle PDRN Cream	SILICON DIOXIDE	Guangzhou Shengyanghui Industrial Trading Co., Ltd	48e2edae-94ea-c42e-e063-6394a90a907b	2026-01-21	Warnings	Exact identifier unii: ETJ7Z6XBU4
Inflammation I	ECHINACEA (ANGUSTIFOLIA), NASTURTIUM AQUATICUM, PHYTOLACCA DECANDRA, HYDRASTIS CANADENSIS, APIS MELLIFICA, BELLADONNA, FERRUM PHOSPHORICUM, NITRICUM ACIDUM, OLEANDER, SILICEA	BioActive Nutritional, Inc.	3cb12181-ae7e-45c7-a1b1-e1952f36f8c3	2026-01-21	Warnings	Exact identifier unii: ETJ7Z6XBU4
Ketoconazole	KETOCONAZOLE CREAM, 2%	Sportpharm LLC	d68f090d-82ea-413f-ab76-9254a8888736	2026-01-19	Warnings, Adverse reactions	Exact identifier unii: R9400W927I
DENTI BUONGIORNO PLAQUE CARE LEMON MINT TOOTH	SILICA, SODIUM FLUORIDE, TOCOPHERYL ACETATE, TETRASODIUM PYROPHOSPHATE	ATOSAFE CO., Ltd	487c5036-0eb0-ada9-e063-6394a90aa02e	2026-01-16	Warnings	Exact identifier unii: ETJ7Z6XBU4
DENTI BUONGIORNO PLAQUE CARE LEMON MINT TOOTH	SILICA, SODIUM FLUORIDE, TOCOPHERYL ACETATE, TETRASODIUM PYROPHOSPHATE	DONG IL PHARMS CO.,LTD	487cd5b9-28f3-392d-e063-6394a90a9ba1	2026-01-16	Warnings	Exact identifier unii: ETJ7Z6XBU4
DENTI BUONGIORNO GUM CARE COOL MINT TOOTH	SILICA, SODIUM FLUORIDE, TOCOPHERYL ACETATE	ATOSAFE CO., Ltd	487cf27a-d761-6353-e063-6394a90af029	2026-01-16	Warnings	Exact identifier unii: ETJ7Z6XBU4
DENTI BUONGIORNO FRESH BREATH HERB MINT TOOTH	SILICA, SODIUM MONOFLUOROPHOSPHATE	ATOSAFE CO., Ltd	487d52d1-8853-bc90-e063-6394a90ab91d	2026-01-16	Warnings	Exact identifier unii: ETJ7Z6XBU4
DENTI BUONGIORNO GUM CARE COOL MINT TOOTH	SILICA, SODIUM FLUORIDE, TOCOPHERYL ACETATE	DONG IL PHARMS CO.,LTD	487d689d-ebdd-43c3-e063-6294a90af0e2	2026-01-16	Warnings	Exact identifier unii: ETJ7Z6XBU4
DENTI BUONGIORNO FRESH BREATH HERB MINT TOOTH	SILICA, SODIUM MONOFLUOROPHOSPHATE	DONG IL PHARMS CO.,LTD	487da363-1d01-8cdc-e063-6294a90ac24d	2026-01-16	Warnings	Exact identifier unii: ETJ7Z6XBU4
Lotrimin Daily Sweat and Odor Control	TOPICAL STARCH	Bayer HealthCare LLC.	9ec5c80d-b550-496f-e053-2a95a90a5489	2026-01-16	Warnings	Exact identifier unii: O8232NY3SJ
Berberis Quartz	BERBERIS QUARTZ	Uriel Pharmacy Inc.	5da48d70-1140-495d-b672-0e55c04196e1	2026-01-16	Warnings	Exact identifier unii: ETJ7Z6XBU4
Anti-Fungal	ANTI-FUNGAL SHAMPOO	Shenzhen Mengyue Technology Co., Ltd.	482c0243-1073-f578-e063-6294a90adf5c	2026-01-15	Warnings	Exact identifier unii: R9400W927I
Constipation Relief	ALUMINUM OXIDE, BRYONIA ALBA ROOT, SODIUM CHLORIDE, GRAPHITE, SILICON DIOXIDE	Homeocare Laboratories	62374240-cd14-44e2-9405-5f8996faf047	2026-01-12	Warnings	Exact identifier unii: ETJ7Z6XBU4
Menopause Relief	BARIUM CARBONATE, ATROPA BELLADONNA, BLACK COHOSH, NITROGLYCERIN, LACHESIS MUTA VENOM, SILICON DIOXIDE	Homeocare Laboratories	99b182d5-4102-4b25-85d3-f4be077d753f	2026-01-12	Warnings	Exact identifier unii: ETJ7Z6XBU4
Amber Amethyst	AMBER AMETHYST	Uriel Pharmacy, Inc	4837e805-a777-c1fa-e063-6294a90ae9c4	2026-01-12	Warnings	Exact identifier unii: ETJ7Z6XBU4
ECHINACEA	ECHINACEA ANGUSTIFOLIA, HAMAMMELIS VIRGINIANA, CALCAREA PHOSPHORICA, HYDRASTIS CANADANESIS, SENEGA OFFICINALIS, SILICEA, CONIUM, AURUM MURIATICUM NATRONATUM, CALCAREA CARBONICA, FUCUS VESICULOSUS, LACHESIS MUTUS	Marco Pharma International LLC.	7efadb70-99e4-428b-a8ef-a2797327c6fa	2026-01-12	Warnings	Exact identifier unii: ETJ7Z6XBU4
RET Stomach 7001	RET STOMACH	Professional Complementary Health Formulas	086427e0-599e-4405-a996-d949023f9d90	2026-01-08	Warnings	Exact identifier unii: ETJ7Z6XBU4
Organophosphate Combination 9309	ORGANOPHOSPHATE COMBINATION	Professional Complementary Health Formulas	f777015f-1df6-4821-af63-543175313aba	2026-01-08	Warnings	Exact identifier unii: ETJ7Z6XBU4
Low Vaccinosis Nosode 4024	LOW VACCINOSIS NOSODE	Professional Complementary Health Formulas	f347ac8f-ac05-46ef-91a3-9f7e00034768	2026-01-08	Warnings	Exact identifier unii: ETJ7Z6XBU4
First Chakra (Root) 7301	FIRST CHAKRA (ROOT)	Professional Complementary Health Formulas	61eb1bbe-6675-4369-b852-18975e6b08c7	2026-01-08	Warnings	Exact identifier unii: ETJ7Z6XBU4

Reported adverse events (FAERS/openFDA)#

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