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 119 of 136 · 2,713 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Farmasi BB Beauty Balm Cream SPF 15- 02 Light to Medium	TITANIUM DIOXIDE	Farmasi US LLC	cef1a926-b7d4-47d6-957d-e3092e60970c	2023-11-05	Warnings	Exact identifier unii: 15FIX9V2JP
Farmasi BB Beauty Balm Cream SPF 15- 06 Deep	TITANIUM DIOXIDE	Farmasi US LLC	2f13a160-740f-4b09-8858-e438a9ba303e	2023-11-05	Warnings	Exact identifier unii: 15FIX9V2JP
Farmasi BB Beauty Balm Cream SPF 15- 05 Tan	TITANIUM DIOXIDE	Farmasi US LLC	3f494921-844e-4010-ab0c-144c8dce8aca	2023-11-05	Warnings	Exact identifier unii: 15FIX9V2JP
Farmasi CC Color Control Cream SPF 25	TITANIUM DIOXIDE	Farmasi US LLC	f4fcfc78-9591-4a20-b9fb-88e1dc9b221d	2023-11-05	Warnings	Exact identifier unii: 15FIX9V2JP
Farmasi CC Color Control Cream SPF 25- 02 Light to Medium	TITANIUM DIOXIDE	Farmasi US LLC	0d913242-2e57-4ba7-a718-154af68480b2	2023-11-05	Warnings	Exact identifier unii: 15FIX9V2JP
Farmasi BB Beauty Balm Cream SPF 15- 03 Medium	TITANIUM DIOXIDE	Farmasi US LLC	6ef986df-4044-4c32-8b64-f8110c9c9543	2023-11-05	Warnings	Exact identifier unii: 15FIX9V2JP
Farmasi CC Color Control Cream SPF 25- 04 Medium to Tan	TITANIUM DIOXIDE	Farmasi US LLC	de24317f-2cf0-4125-bb17-c3d6b3c22e00	2023-11-05	Warnings	Exact identifier unii: 15FIX9V2JP
Farmasi CC Color Control Cream SPF 25- 05 Tan	TITANIUM DIOXIDE	Farmasi US LLC	22842793-ae1f-4b71-8db9-34c06dc37daa	2023-11-05	Warnings	Exact identifier unii: 15FIX9V2JP
Farmasi CC Color Control Cream SPF 25- 03 Medium	TITANIUM DIOXIDE	Farmasi US LLC	9f203e7f-3bba-4f36-a35a-6d9466e39082	2023-11-05	Warnings	Exact identifier unii: 15FIX9V2JP
Farmasi CC Color Control Cream SPF 25- 06 Deep	TITANIUM DIOXIDE	Farmasi US LLC	c28afa3b-9a8d-4e19-bc6b-39cc8428c9f9	2023-11-05	Warnings	Exact identifier unii: 15FIX9V2JP
PHARMACA Natural Mineral Sunscreen SPF-50	TITANIUM DIOXIDE, ZINC OXIDE	Pharmaca Integrative Pharmacy, Inc.	51e6cd7a-5c9a-4666-9021-ade42eb064cd	2023-11-05	Warnings	Exact identifier unii: 15FIX9V2JP
VERTRA Premium Suncare SPF 30	TITANIUM DIOXIDE, ZINC OXIDE	Eai-Jr286, Inc.	720ca725-24ca-4b59-b640-afa983238692	2023-11-05	Warnings	Exact identifier unii: 15FIX9V2JP
FOREVER Transfer-proof 24h foundation High perfection Concentrated floral skincare with sunscreen Broad spectrum SPF 15 1C	OCTISALATE, TITANIUM DIOXIDE	Parfums Christian Dior	4c9ffd30-4799-475d-94cb-07ce3d5b3660	2023-11-04	Warnings	Exact identifier unii: 15FIX9V2JP
Leg Cramps-Swelling	ECHINACEA, ARGENTUM NITRICUM, BRYONIA, CALCAREA CARBONICA, COLOCYNTHIS, CONVALLARIA MAJALIS, CROTALUS HORRIDUS, CUPRUM METALLICUM, DIGITALIS , GELSEMIUM SEMPERVIRENS, HYPERICUM PERFORATUM, KALI CARBONICUM, LACHESIS MUTUS, LATHYRUS SATIVUS, LILIUM TIGRINUM, MAGNESIA PHOSPHORICA, NUX VOMICA, RHUS TOXICODENDRON, SILICEA, STRAMONIUM, VERATRUM VIRIDE, ELAPS	Newton Laboratories, Inc.	9c31d465-caac-3a02-e053-2a95a90adb3b	2023-11-03	Warnings	Exact identifier unii: ETJ7Z6XBU4
Youth 2 Activating BB Cream SPF 30 Light Medium	ZINC OXIDE, TITANIUM DIOXIDE	Shaklee Corporation	e51e38c9-cc9b-4af3-842d-41d0162f17ff	2023-11-03	Warnings	Exact identifier unii: 15FIX9V2JP
Youth 4 Activating BB Cream SPF 30 Dark	ZINC OXIDE, TITANIUM DIOXIDE	Shaklee Corporation	63f7f8bd-02f0-4a13-bb1e-298754b24fce	2023-11-03	Warnings	Exact identifier unii: 15FIX9V2JP
Youth 1 Activating BB Cream SPF 30 Light	ZINC OXIDE, TITANIUM DIOXIDE	Shaklee Corporation	c9e05055-48ea-405d-b1d4-50b263d0dbf9	2023-11-03	Warnings	Exact identifier unii: 15FIX9V2JP
CAPTURE DREAMSKIN FRESH and PERFECT CUSHION WITH SUNSCREEN BROAD SPECTRUM SPF 50 020	OCTINOXATE,TITANIUM DIOXIDE,ZINC OXIDE	Parfums Christian Dior	fe03fc14-4132-4dab-b013-d490764be0d4	2023-11-03	Warnings	Exact identifier unii: 15FIX9V2JP
CAPTURE DREAMSKIN FRESH and PERFECT CUSHION WITH SUNSCREEN BROAD SPECTRUM SPF 50 000	OCTINOXATE,TITANIUM DIOXIDE,ZINC OXIDE	Parfums Christian Dior	968cfae7-89b6-4ef3-ab60-1c675b90c151	2023-11-03	Warnings	Exact identifier unii: 15FIX9V2JP
CAPTURE DREAMSKIN FRESH and PERFECT CUSHION WITH SUNSCREEN BROAD SPECTRUM SPF 50 010	OCTINOXATE,TITANIUM DIOXIDE,ZINC OXIDE	Parfums Christian Dior	775f4009-9fc2-475b-a141-b4b5e5542180	2023-11-03	Warnings	Exact identifier unii: 15FIX9V2JP

Reported adverse events (FAERS/openFDA)#

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