NDC 51672-4002-01 - Nortriptyline Hydrochloride

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: 51672-4002
Requested NDC: 51672-4002-01
Package NDCs from labels: 51672-4002-6, 51672-4002-4, 51672-4002-5, 51672-4002-1, 51672-4002-2, 51672-4002-01
Manufacturer: Bryant Ranch Prepack
Effective date: 2026-08-18
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Nortriptyline Hydrochloride - Bryant Ranch Prepack	Bryant Ranch Prepack	2026-08-18	HUMAN PRESCRIPTION DRUG LABEL
Nortriptyline Hydrochloride Capsules, USP	Sun Pharmaceutical Industries, Inc. \| Taro Pharmaceutical Industries, Ltd.	2026-07-15	HUMAN PRESCRIPTION DRUG LABEL
Nortriptyline Hydrochloride - Northwind Health Company, LLC	Northwind Health Company, LLC	2026-01-01	HUMAN PRESCRIPTION DRUG LABEL
Nortriptyline Hydrochloride - Quality Care Products LLC	Quality Care Products LLC	2024-12-17	HUMAN PRESCRIPTION DRUG LABEL
Nortriptyline Hydrochloride - American Health Packaging	American Health Packaging	2024-08-07	HUMAN PRESCRIPTION DRUG LABEL
Nortriptyline Hydrochloride Capsules, USP	NuCare Pharmaceuticals, Inc. \| NuCarePharmaceuticals, Inc.	2024-07-19	HUMAN PRESCRIPTION DRUG LABEL
Nortriptyline Hydrochloride Capsules, USP	PD-Rx Pharmaceuticals, Inc.	2024-03-25	HUMAN PRESCRIPTION DRUG LABEL
Nortriptyline Hydrochloride - A-S Medication Solutions	A-S Medication Solutions	2024-03-17	HUMAN PRESCRIPTION DRUG LABEL
Nortriptyline Hydrochloride Capsules, USP	REMEDYREPACK INC.	2024-02-13	HUMAN PRESCRIPTION DRUG LABEL
Nortriptyline Hydrochloride - AvPAK	AvPAK	2024-01-08	HUMAN PRESCRIPTION DRUG LABEL
NORTRIPTYLINE HCI - Direct_Rx	Direct_Rx	2022-10-05	HUMAN PRESCRIPTION DRUG LABEL
NORTRIPTYLINE HCI - Direct_Rx	Direct_Rx	2022-10-05	HUMAN PRESCRIPTION DRUG LABEL
Nortriptyline Hydrochloride Capsules, USP	Preferred Pharmaceuticals Inc.	2022-09-14	HUMAN PRESCRIPTION DRUG LABEL
Nortriptyline Hydrochloride Capsules, USP	REMEDYREPACK INC.	2022-07-06	HUMAN PRESCRIPTION DRUG LABEL
Nortriptyline Hydrochloride - Proficient Rx LP	Proficient Rx LP	2022-07-01	HUMAN PRESCRIPTION DRUG LABEL
Nortriptyline Hydrochloride - Clinical Solutions Wholesale, LLC	Clinical Solutions Wholesale, LLC	2020-07-26	HUMAN PRESCRIPTION DRUG LABEL
Nortriptyline HCL - Direct_Rx	Direct_Rx	2019-03-11	HUMAN PRESCRIPTION DRUG LABEL
Nortriptyline Hydrochloride Capsules, USP	St. Mary's Medical Park Pharmacy \| Taro Pharmaceutical Industries, Ltd.	2018-11-16	HUMAN PRESCRIPTION DRUG LABEL
Nortriptyline Hydrochloride - Unit Dose Services	Unit Dose Services	2018-04-19	HUMAN PRESCRIPTION DRUG LABEL
Nortriptyline Hydrochloride - Aidarex Pharmaceuticals LLC	Aidarex Pharmaceuticals LLC	2016-11-03	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
51672-4002-1	Nortriptyline Hydrochloride	100 in 1 BOTTLE	CAPSULE	100	10
51672-4002-2	Nortriptyline Hydrochloride	500 in 1 BOTTLE	CAPSULE	500	10
51672-4002-4	Nortriptyline Hydrochloride	60 in 1 BOTTLE	CAPSULE	60	10
51672-4002-5	Nortriptyline Hydrochloride	90 in 1 BOTTLE	CAPSULE	90	10
51672-4002-6	Nortriptyline Hydrochloride	30 in 1 BOTTLE	CAPSULE	30	10

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
51672-4002	NORTRIPTYLINE HYDROCHLORIDE CAPSULE [TARO PHARMACEUTICALS U.S.A., INC.]	10	Current NDC, Legacy NDC, 5 package rows	20200508_aee2c1a1-d848-4c3b-8c6d-8a4f6ce94c28.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
51672-4002-1	EA - Each	51672-4002	aa566477-3aad-44a5-ad7c-6be836523d6b	1	2016-02-04
51672-4002-5	EA - Each	51672-4002	217e5126-c662-4b12-8e51-06da3c2afc45	1	2013-02-13
51672-4002-6	EA - Each	51672-4002	9481fdef-5327-4e13-bb32-e582e0beaed6	1	2013-02-13

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
Nortriptyline Hydrochloride	ACTIVE INGREDIENT	00FN6IH15D	NORTRIPTYLINE HYDROCHLORIDE CAPSULE [TARO PHARMACEUTICALS U.S.A., INC.]	8
Nortriptyline	ACTIVE MOIETY	BL03SY4LXB	NORTRIPTYLINE HYDROCHLORIDE CAPSULE [TARO PHARMACEUTICALS U.S.A., INC.]	8
aluminum oxide	INACTIVE INGREDIENT	LMI26O6933	NORTRIPTYLINE HYDROCHLORIDE CAPSULE [TARO PHARMACEUTICALS U.S.A., INC.]	8
D&C Yellow NO. 10	INACTIVE INGREDIENT	35SW5USQ3G	NORTRIPTYLINE HYDROCHLORIDE CAPSULE [TARO PHARMACEUTICALS U.S.A., INC.]	8
FD&C Blue NO. 1	INACTIVE INGREDIENT	H3R47K3TBD	NORTRIPTYLINE HYDROCHLORIDE CAPSULE [TARO PHARMACEUTICALS U.S.A., INC.]	8
FD&C Blue NO. 2	INACTIVE INGREDIENT	L06K8R7DQK	NORTRIPTYLINE HYDROCHLORIDE CAPSULE [TARO PHARMACEUTICALS U.S.A., INC.]	8
FD&C Green NO. 3	INACTIVE INGREDIENT	3P3ONR6O1S	NORTRIPTYLINE HYDROCHLORIDE CAPSULE [TARO PHARMACEUTICALS U.S.A., INC.]	8
FD&C Red NO. 40	INACTIVE INGREDIENT	WZB9127XOA	NORTRIPTYLINE HYDROCHLORIDE CAPSULE [TARO PHARMACEUTICALS U.S.A., INC.]	8
ferrosoferric oxide	INACTIVE INGREDIENT	XM0M87F357	NORTRIPTYLINE HYDROCHLORIDE CAPSULE [TARO PHARMACEUTICALS U.S.A., INC.]	8
gelatin	INACTIVE INGREDIENT	2G86QN327L	NORTRIPTYLINE HYDROCHLORIDE CAPSULE [TARO PHARMACEUTICALS U.S.A., INC.]	8
magnesium stearate	INACTIVE INGREDIENT	70097M6I30	NORTRIPTYLINE HYDROCHLORIDE CAPSULE [TARO PHARMACEUTICALS U.S.A., INC.]	8
shellac	INACTIVE INGREDIENT	46N107B71O	NORTRIPTYLINE HYDROCHLORIDE CAPSULE [TARO PHARMACEUTICALS U.S.A., INC.]	8
silicon dioxide	INACTIVE INGREDIENT	ETJ7Z6XBU4	NORTRIPTYLINE HYDROCHLORIDE CAPSULE [TARO PHARMACEUTICALS U.S.A., INC.]	8
sodium lauryl sulfate	INACTIVE INGREDIENT	368GB5141J	NORTRIPTYLINE HYDROCHLORIDE CAPSULE [TARO PHARMACEUTICALS U.S.A., INC.]	8
starch, corn	INACTIVE INGREDIENT	O8232NY3SJ	NORTRIPTYLINE HYDROCHLORIDE CAPSULE [TARO PHARMACEUTICALS U.S.A., INC.]	8
titanium dioxide	INACTIVE INGREDIENT	15FIX9V2JP	NORTRIPTYLINE HYDROCHLORIDE CAPSULE [TARO PHARMACEUTICALS U.S.A., INC.]	8
Nortriptyline Hydrochloride	ACTIVE INGREDIENT	00FN6IH15D	NORTRIPTYLINE HYDROCHLORIDE CAPSULE [PREFERRED PHARMACEUTICALS INC.]	1
Nortriptyline	ACTIVE MOIETY	BL03SY4LXB	NORTRIPTYLINE HYDROCHLORIDE CAPSULE [PREFERRED PHARMACEUTICALS INC.]	1
aluminum oxide	INACTIVE INGREDIENT	LMI26O6933	NORTRIPTYLINE HYDROCHLORIDE CAPSULE [PREFERRED PHARMACEUTICALS INC.]	1
D&C Yellow NO. 10	INACTIVE INGREDIENT	35SW5USQ3G	NORTRIPTYLINE HYDROCHLORIDE CAPSULE [PREFERRED PHARMACEUTICALS INC.]	1
FD&C Blue NO. 1	INACTIVE INGREDIENT	H3R47K3TBD	NORTRIPTYLINE HYDROCHLORIDE CAPSULE [PREFERRED PHARMACEUTICALS INC.]	1
FD&C Blue NO. 2	INACTIVE INGREDIENT	L06K8R7DQK	NORTRIPTYLINE HYDROCHLORIDE CAPSULE [PREFERRED PHARMACEUTICALS INC.]	1
FD&C Red NO. 40	INACTIVE INGREDIENT	WZB9127XOA	NORTRIPTYLINE HYDROCHLORIDE CAPSULE [PREFERRED PHARMACEUTICALS INC.]	1
ferrosoferric oxide	INACTIVE INGREDIENT	XM0M87F357	NORTRIPTYLINE HYDROCHLORIDE CAPSULE [PREFERRED PHARMACEUTICALS INC.]	1
gelatin	INACTIVE INGREDIENT	2G86QN327L	NORTRIPTYLINE HYDROCHLORIDE CAPSULE [PREFERRED PHARMACEUTICALS INC.]	1
magnesium stearate	INACTIVE INGREDIENT	70097M6I30	NORTRIPTYLINE HYDROCHLORIDE CAPSULE [PREFERRED PHARMACEUTICALS INC.]	1
shellac	INACTIVE INGREDIENT	46N107B71O	NORTRIPTYLINE HYDROCHLORIDE CAPSULE [PREFERRED PHARMACEUTICALS INC.]	1
silicon dioxide	INACTIVE INGREDIENT	ETJ7Z6XBU4	NORTRIPTYLINE HYDROCHLORIDE CAPSULE [PREFERRED PHARMACEUTICALS INC.]	1
sodium lauryl sulfate	INACTIVE INGREDIENT	368GB5141J	NORTRIPTYLINE HYDROCHLORIDE CAPSULE [PREFERRED PHARMACEUTICALS INC.]	1
starch, corn	INACTIVE INGREDIENT	O8232NY3SJ	NORTRIPTYLINE HYDROCHLORIDE CAPSULE [PREFERRED PHARMACEUTICALS INC.]	1
titanium dioxide	INACTIVE INGREDIENT	15FIX9V2JP	NORTRIPTYLINE HYDROCHLORIDE CAPSULE [PREFERRED PHARMACEUTICALS INC.]	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 86 of 137 · 2,727 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Stay Ageless Tinted Mineral Sunscreen Broad Spectrum SPF 30	TITANIUM DIOXIDE AND ZINC OXIDE	BEAUTY SENSE MEDSPA INC	fe93a337-8d2f-35d3-e053-6294a90acb3c	2025-01-08	Warnings	Exact identifier unii: 15FIX9V2JP
Sunscreen Emulsion SPF50plus	OCTOCRYLENE,ETHYLHEXYL METHOXYCIRNNAMATE,TITANIUM DIOXIDE,ETHYLHEXYL SALICYLATE	Guangzhou Senmai Biotechnology Co.	1d560670-026b-bd34-e063-6394a90a9af4	2025-01-08	Warnings	Exact identifier unii: 15FIX9V2JP
Ferrum Silicicum Urtica	FERRUM SILICICUM URTICA	Uriel Pharmacy Inc.	09829ac4-c074-7315-e063-6394a90adf59	2025-01-07	Warnings	Exact identifier unii: ETJ7Z6XBU4
Chemtox	TRITICUM AESTIVUM, BERBERIS VULGARIS, GLYCYRRHIZA GLABRA, LAPPA MAJOR, RHAMNUS FRANGULA, RHAMNUS PURSHIANA, STILLINGIA SYLVATICA, TRIFOLIUM PRATENSE, XANTHOXYLUM FRAXINEUM, PHYTOLACCA DECANDRA, GLANDULA SUPRARENALIS SUIS, HEPAR SUIS, LYMPH NODE (SUIS), THYROIDINUM (SUIS), BELLADONNA, LYCOPODIUM CLAVATUM, NITRICUM ACIDUM, NUX VOMICA, PHOSPHORICUM ACIDUM, PHOSPHORUS, SALICYLICUM ACIDUM, CORTISONE ACETICUM, EUGENOL, STEARYL ALCOHOL, XYLITOL, FOLLICULINUM, BENZOICUM ACIDUM, CHLORINUM, POTASSIUM SORBATE,	BioActive Nutritional, Inc.	a480e5f4-5f9e-4b23-b257-b0ac1ebfc115	2025-01-07	Warnings	Exact identifier unii: LKG8494WBH
sunbetter Broad Spectrum SPF 56 Sunscreen Stick Sheer	ZINC OXIDE, TITANIUM DIOXIDE	SKINBETTER SCIENCE LLC	92c4e4cb-aadc-26f4-e053-2995a90a03d5	2025-01-06	Warnings	Exact identifier unii: 15FIX9V2JP
sunbetter Broad Spectrum SPF 56 Sunscreen Compact Sheer	ZINC OXIDE, TITANIUM DIOXIDE	SKINBETTER SCIENCE LLC	b8a4986d-c28f-c4f4-e053-2a95a90a7167	2025-01-06	Warnings	Exact identifier unii: 15FIX9V2JP
sunbetter Broad Spectrum SPF 68 Sunscreen Compact Tone Smart	ZINC OXIDE, TITANIUM DIOXIDE	SKINBETTER SCIENCE LLC	8f119447-045b-43f3-e053-2995a90aea77	2025-01-06	Warnings	Exact identifier unii: 15FIX9V2JP
sunbetter Broad Spectrum SPF 75 Sunscreen Tone Smart	ZINC OXIDE, TITANIUM DIOXIDE	SKINBETTER SCIENCE LLC	b878ee3b-6897-3c4a-e053-2995a90afed7	2025-01-06	Warnings	Exact identifier unii: 15FIX9V2JP
sunbetter Broad Spectrum SPF 70 Sunscreen Sheer	ZINC OXIDE, TITANIUM DIOXIDE	SKINBETTER SCIENCE LLC	b879067b-9d7f-3a62-e053-2995a90a9d6b	2025-01-06	Warnings	Exact identifier unii: 15FIX9V2JP
glo SKIN BEAUTY Luminous Liquid Foundation SPF 18	GLO SKIN BEAUTY LUMINOUS LIQUID FOUNDATION SPF 18	Hayden Caleel LLC	dd863361-281d-45fe-a8c1-6e4c670809a5	2025-01-05	Warnings	Exact identifier unii: 15FIX9V2JP
Dr.Jucre Rebirth BB	TITANIUM DIOXIDE, OCTINOXATE, ZINC OXIDE, NIACINAMIDE, ADENOSINE	NATURECELL CO., LTD.	2ab403df-29b3-75af-e063-6394a90a6ca4	2025-01-02	Warnings	Exact identifier unii: 15FIX9V2JP
Green Defense Broad Spectrum SPF 30	TITANIUM DIOXIDE, ZINC OXIDE	Farmacy Beauty LLC	adf0f50f-6357-bc1f-e053-2a95a90ad997	2025-01-02	Warnings	Exact identifier unii: 15FIX9V2JP
MIMIBO PREMIUM TOOTH	SILICON DIOXIDE, TOCOPHEROL ACETATE, TETRASODIUM PYROPHOSPHATE	CONE MEDICAL Co., Ltd.	c0ff5df4-0b37-0b1b-e053-2a95a90a862c	2025-01-02	Warnings	Exact identifier unii: ETJ7Z6XBU4
MIMIBO PREMIUM TOOTH	SILICON DIOXIDE, TOCOPHEROL ACETATE, TETRASODIUM PYROPHOSPHATE	CONE MEDICAL Co., Ltd.	c101881a-5a12-2e04-e053-2a95a90a3f57	2025-01-02	Warnings	Exact identifier unii: ETJ7Z6XBU4
Exel Clarifying Line Daily Fluid Sun Shield white color Broad Spectrum SPF 60 plus	OCTOCRYLENE, OCTINOXATE, OCTISALATE, TITANIUM DIOXIDE, ENSULIZOLE	Exelencia importers Corp.	283c2780-5ad5-38f1-e063-6294a90ac336	2025-01-01	Warnings	Exact identifier unii: 15FIX9V2JP
EXEL CLARIFYING LINE DAILY FLUID SUN SHIELD WHITE COLOR BROAD SPECTRUM SPF 60 PLUS	OCTOCRYLENE, OCTINOXATE, OCTISALATE, TITANIUM DIOXIDE, ENSULIZOLE	Biocosmetica Exel Argentina SRL	2aabf782-65f9-e894-e063-6394a90a1ea3	2025-01-01	Warnings	Exact identifier unii: 15FIX9V2JP
EXEL CLARIFYING LINE DAILY FLUID SUN SHIELD WALNUT BROWN COLOR BROAD SPECTRUM SPF 60 PLUS	OCTOCRYLENE, OCTINOXATE, OCTISALATE, TITANIUM DIOXIDE, ENSULIZOLE	Biocosmetica Exel Argentina SRL	2aad5b97-e64b-c678-e063-6294a90aa8c6	2025-01-01	Warnings	Exact identifier unii: 15FIX9V2JP
NativeRemedies Acid Free-Flux	CALC PHOS 9X, CARBO VEG 6C, MAG CARB 6C, NAT PHOS 9X, SILICEA 9X	Silver Star Brands	d5012b1f-861e-40b8-e053-2a95a90a4fe2	2025-01-01	Warnings	Exact identifier unii: ETJ7Z6XBU4
Mucus Clear Allergy Relief	ALLIU CEPA, CALC PHOS, EUPHRASIA, IGNATIA, KALI MUR, NAT MUR, NUX VOM, PULSATILLA, SILICA	Silver Star Brands	f49bdcc1-1939-6dc2-e053-2995a90a0a3b	2025-01-01	Warnings	Exact identifier unii: ETJ7Z6XBU4
NativeRemedies Gout-Gone	ANTIMON CRUD, BENZOICUM AC, LEDUM, NUX VOM, QUERCUS, RHODODENDRON, SILICEA	Silver Star Brands	f66b42f0-8f5f-1aca-e053-2a95a90ae396	2025-01-01	Warnings	Exact identifier unii: ETJ7Z6XBU4

Reported adverse events (FAERS/openFDA)#

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