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 64 of 137 · 2,727 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
ALUMIZEN	GARLIC, AVENA SATIVA FLOWERING TOP, BERBERIS VULGARIS ROOT BARK, ARCTIUM LAPPA ROOT, PHYTOLACCA AMERICANA ROOT, SOLIDAGO VIRGAUREA FLOWERING TOP, ALUMINUM OXIDE, SILVER NITRATE, BARIUM CARBONATE, BERYLLIUM, CADMIUM, COPPER, HYDROFLUORIC ACID, INDIUM, IODINE, LITHIUM CARBONATE, MERCURIUS SOLUBILIS, NICKEL CARBONATE HYDROXIDE TETRAHYDRATE, NITROUS OXIDE, LEAD, SELENIUM, STRONTIUM CARBONATE, TITANIUM, ARSENIC TRIOXIDE, SODIUM CHLORIDE, STRYCHNOS NUX-VOMICA SEED.	Natural Creations, Inc.	4760ab09-1141-4944-b840-804ae6d86d2d	2025-11-13	Warnings	Exact identifier unii: LMI26O6933
Glo Skin	TITANIUM DIOXIDE, ZINC OXIDE	Glo Skin Beauty	f4bed574-68c1-0d2c-e053-2a95a90a15ff	2025-11-13	Warnings	Exact identifier unii: 15FIX9V2JP
BELLA HP	ATROPA BELLADONNA, CONIUM MACULATUM FLOWERING TOP, SOLANUM DULCAMARA TOP, CALCIUM SULFIDE, POTASSIUM DICHROMATE, MERCURIUS SOLUBILIS, ANEMONE PULSATILLA, SILICON DIOXIDE, MATRICARIA RECUTITA.	Natural Creations, Inc.	8e46906b-9c22-4a8e-ae4e-f1fbfb3d35b1	2025-11-13	Warnings	Exact identifier unii: ETJ7Z6XBU4
BONE HP	SODIUM BORATE, OYSTER SHELL CALCIUM CARBONATE CRUDE, CALCIUM FLUORIDE, TRIBASIC CALCIUM PHOSPHATE, EUPATORIUM PERFOLIATUM FLOWERING TOP, IRON, HYDROFLUORIC ACID, HEKLA LAVA, TOXICODENDRON PUBESCENS LEAF, RUTA GRAVEOLENS FLOWERING TOP, SILICON DIOXIDE, COMFREY ROOT.	Natural Creations, Inc.	93d2b385-9ce3-4d16-b428-1638e9a55f92	2025-11-13	Warnings	Exact identifier unii: ETJ7Z6XBU4
43533575-ce3e-bce8-e063-6294a90a2152			bdfac553-db8d-4bbd-b663-a03f57876867	2025-11-11	Boxed warning, Warnings, Adverse reactions	Exact identifier spl set id: bdfac553-db8d-4bbd-b663-a03f57876867
Essential Defense Mineral Shield Broad Spectrum SPF 32 Sunscreen TINTED	TITANIUM DIOXIDE AND ZINC OXIDE	Allergan, Inc.	279a5214-79b2-44e9-b003-378d0b992395	2025-11-11	Warnings	Exact identifier unii: 15FIX9V2JP
buttah Tinted Mineral Sunscreen SPF-30	TITANIUM DIOXIDE, ZINC OXIDE	Buttah Enterprises, LLC.	43458152-0775-dd9c-e063-6394a90a6140	2025-11-10	Warnings	Exact identifier unii: 15FIX9V2JP
LUMOe SKIN1 Skin Remedy	KALI MURIATICUM, PRUNUS SPINOSA, SILICEA, SARSAPARILLA	Applied Bioenergetics, LLC	d4d7fd2f-66bf-407d-ad36-2462e880b9f5	2025-11-10	Warnings	Exact identifier unii: ETJ7Z6XBU4
Walgreens SPF 50 Tinted Mineral Fluid	TITANIUM DIOXIDE	Walgreens	345918e3-95f8-404c-e063-6394a90a3fca	2025-11-09	Warnings	Exact identifier unii: 15FIX9V2JP
Ananassa Resina	ANANASSA RESINA	Uriel Pharmacy Inc.	52a18d0a-2c97-4e81-81ff-c836582d0a4c	2025-11-07	Warnings	Exact identifier unii: ETJ7Z6XBU4
e.l.f Camo Semi-Matte CC Cream SPF 30 Deep 500 W	ZINC OXIDE, TITANIUM DIOXIDE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	e.l.f. Cosmetics, Inc.	d690d5d1-e1fa-404f-a17e-7b97be17b44a	2025-11-07	Warnings	Exact identifier unii: 15FIX9V2JP
e.l.f Camo Semi-Matte CC Cream SPF 30 Deep 510 C	ZINC OXIDE, TITANIUM DIOXIDE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	e.l.f. Cosmetics, Inc.	2fbdeff7-4880-49ef-bb4d-e033d18e0459	2025-11-07	Warnings	Exact identifier unii: 15FIX9V2JP
e.l.f Camo Semi-Matte CC Cream SPF 30 Deep 540 N	ZINC OXIDE, TITANIUM DIOXIDE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	e.l.f. Cosmetics, Inc.	6a86e5fd-6736-45e0-aa7d-d268fdaed4f8	2025-11-07	Warnings	Exact identifier unii: 15FIX9V2JP
e.l.f Camo Semi-Matte CC Cream SPF 30 Deep 560 C	ZINC OXIDE, TITANIUM DIOXIDE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	e.l.f. Cosmetics, Inc.	42a3625f-5c58-4ec5-895f-b14f74428271	2025-11-07	Warnings	Exact identifier unii: 15FIX9V2JP
e.l.f Camo Semi-Matte CC Cream SPF 30 Tan 415 C	ZINC OXIDE, TITANIUM DIOXIDE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	e.l.f. Cosmetics, Inc.	8e14fe81-cf7f-4a81-afec-e6c8466179c9	2025-11-07	Warnings	Exact identifier unii: 15FIX9V2JP
e.l.f Camo Semi-Matte CC Cream SPF 30 Tan 425 N	ZINC OXIDE, TITANIUM DIOXIDE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	e.l.f. Cosmetics, Inc.	7dd9f4cb-78d8-4edc-a63c-d4a02930a0f8	2025-11-07	Warnings	Exact identifier unii: 15FIX9V2JP
e.l.f Camo Semi-Matte CC Cream SPF 30 Tan 450 N	ZINC OXIDE, TITANIUM DIOXIDE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	e.l.f. Cosmetics, Inc.	8acb660f-94bd-4c4f-b0c1-3682cf8ed543	2025-11-07	Warnings	Exact identifier unii: 15FIX9V2JP
e.l.f Camo Semi-Matte CC SPF 30 Fair 150 C	ZINC OXIDE, TITANIUM DIOXIDE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	e.l.f. Cosmetics, Inc.	fad2bec7-c5f4-45f4-aff4-a5022033cb6a	2025-11-07	Warnings	Exact identifier unii: 15FIX9V2JP
e.l.f Camo Semi-Matte CC SPF 30 Medium 355 W	ZINC OXIDE, TITANIUM DIOXIDE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	e.l.f. Cosmetics, Inc.	39856c69-84fb-4b12-a713-8912263e42b1	2025-11-07	Warnings	Exact identifier unii: 15FIX9V2JP
Nortriptyline Hydrochloride	NORTRIPTYLINE HYDROCHLORIDE	Bryant Ranch Prepack	43a81887-42b8-43b5-b58a-3f3df2e9949b	2025-11-07	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 198045 unii: 00FN6IH15D

Reported adverse events (FAERS/openFDA)#

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