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 | 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 | Form | Quantity | Strength | 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 | 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 | 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#
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.
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| Bambusa Pulsatilla | BAMBUSA PULSATILLA | Uriel Pharmacy Inc. | 0776c3be-088d-422c-9c12-08fcaae823e1 | 2025-11-26 | Warnings | ETJ7Z6XBU4 |
| Thyroid-Adrenal | ADRENALINUM, THYROIDINUM, ALOE, CALC. CARB., CHELIDONIUM MAJUS, CONIUM, GRAPHITES, IODIUM, LACHESIS, LYCOPODIUM, LYCOPUS VIRGINICUS, PHYTOLACCA, RHUS TOXICODENDRON, SILICEA, SPONGIA, ECHINACEA | Newton Laboratories, Inc. | b597504a-c667-225c-e053-2a95a90ac704 | 2025-11-25 | Warnings | ETJ7Z6XBU4 |
| DOCTRUST ONE S Tooth | SODIUM FLUORIDE, DENTAL TYPE SILICA, POTASSIUM NIRATE | DONG IL PHARMS CO.,LTD | 4476923a-48f1-9f72-e063-6394a90a0708 | 2025-11-25 | Warnings | ETJ7Z6XBU4 |
| DOCTRUST K Tooth | SILICON DIOXIDE, SODIUM MONOFLUOROPHOSPHATE | DONG IL PHARMS CO.,LTD | 44768dd1-b132-c33b-e063-6294a90accd4 | 2025-11-25 | Warnings | ETJ7Z6XBU4 |
| salmon colored sunscreen | SALMON COLORED SUNSCREEN | Guangzhou Fantesy Biotechnology Co.,Ltd | 4477964b-28f3-a371-e063-6294a90a4230 | 2025-11-25 | Warnings | 15FIX9V2JP |
| Gout Pain Management | ARNICA MONTANA, URTICA URENS, SILICON DIOXIDE, AND THUJA OCCIDENTALIS LEAF | Forces of Nature | 9276fe9c-d9a2-4cef-986c-5d7d39f2d6a1 | 2025-11-25 | Warnings | ETJ7Z6XBU4 |
| Thermacare Heat Therapy Max Strength Lidocaine Pain Relief Gel | THERMACARE HEAT THERAPY MAX STRENGTH LIDOCAINE PAIN RELIEF GEL | Clarion Brands LLC | 445db02a-c8e8-6ebb-e063-6294a90a4301 | 2025-11-24 | Warnings | LKG8494WBH |
| Natural Eyes Floaters Relief | CHELIDONIUM, EUPHRASIA, KALI SULPH, NATRUM MURIATICUM, PHOSPHORUS, PHYSOSTIGMA, SEPIA, SILICEA | TRP Company | 445dc831-195e-4b25-e063-6294a90a6efd | 2025-11-24 | Warnings | ETJ7Z6XBU4 |
| it cosmetics Bye Bye Foundation Full Coverage Moisturizer with 3D Skin Flex Broad Spectrum SPF 50 Plus UVA UVB Physical Sunscreen All Shades | TITANIUM DIOXIDE AND ZINC OXIDE | L'Oreal USA, Inc. | 86eea4df-4191-4e05-9f05-4a98ef8c2a4d | 2025-11-24 | Warnings | 15FIX9V2JP |
| Lymph HP | ACONITUM NAPELLUS, ARSENICUM ALBUM, BAPTISIA TINCTORIA, BELLADONNA, BRYONIA, CAUSTICUM, ECHINACEA, EUPATORIUM PERFOLIATUM, FERRUM PHOSPHORICUM, GELSEMIUM SEMPERVIRENS, HYDRASTIS CANADENSIS, HYPERICUM PERFORATUM, KALI CARBONICUM, LACHESIS MUTUS, LOBELIA INFLATA, LOMATIUM DISSECTUM, LUNG, NATRUM SULPHURICUM, PHOSPHORUS, PHYTOLACCA DECANDRA, PULSATILLA, PYROGENIUM, RHUS TOX, SILICEA, SULPHUR, SYMPHYTUM OFFICINALE | Energique, Inc. | 17aa9d9c-3d32-4963-91db-d1e96717e7ad | 2025-11-24 | Warnings | ETJ7Z6XBU4 |
| Cetaphil Sun Tinted Face SPF 40 | TITANIUM DIOXIDE, ZINC OXIDE | Galderma Laboratories, L.P. | 22413f93-7219-4726-b741-2392e576b34a | 2025-11-24 | Warnings | 15FIX9V2JP |
| VEIL MINERAL PRIMER SUNSCREEN BROAD SPECTRUM SPF 15 | ZINC OXIDE AND TITANIUM DIOXIDE | Kingdom Animalia, LLC DBA Hourglass Cosmetics | 28e23498-953f-47c0-838c-bbf0e858d903 | 2025-11-24 | Warnings | 15FIX9V2JP |
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| Pneumo Sarcode | TEUCRIUM SCORODONIA, ARSENICUM IODATUM, LUNG (BOVINE), CALCAREA PHOSPHORICA, STANNUM METALLICUM, CARBO VEGETABILIS, PHELLANDRIUM AQUATICUM, SILICEA, SULPHUR | Nutritional Specialties, Inc. | c3a7cf75-723e-4fb9-8ff8-ae8f73a0900d | 2025-11-20 | Warnings | ETJ7Z6XBU4 |
| Gelusil | ALUMINA, MAGNESIA, SIMETHICONE | WellSpring Pharmaceutical Corporation | 92fbeec1-1562-40f3-9734-41f133d494f9 | 2025-11-20 | Warnings | ETJ7Z6XBU4 |
| SULWHASOO PERFECTING CUSHION NO. 25 | OCTINOXATE, TITANIUM DIOXIDE, AND ZINC OXIDE | Amorepacific Corporation | 8d420e4b-c778-3ed4-e053-2995a90a59a9 | 2025-11-20 | Warnings | 15FIX9V2JP |
| Protect Prevent Daily Mineral Sunscreen Broad Spectrum SPF30 | TITANIUM DIOXIDE, ZINC OXIDE | Norwex Usa, Inc. | f527a8c5-b05e-5f3c-e053-2995a90aa1a3 | 2025-11-20 | Warnings | 15FIX9V2JP |
| Cold | BAPTISIA TINCTORIA, ECHINACEA ANGUSTIFOLIA, EUPATORIUM PERFOLIATUM, LOMATIUM DISSECTUM, PUERARIA LOBATA, TRIFOLIUM PRATENSE, PHYTOLACCA DECANDRA, ALLIUM CEPA, ARSENICUM IODATUM, BARYTA CARBONICA, BROMIUM, CALCAREA CARBONICA, KALI MURIATICUM, LACHESIS MUTUS, MERCURIUS SOLUBILIS, SILICEA | Natural Creations, Inc | c45d1d8f-24be-4c13-8c4b-388962421415 | 2025-11-20 | Warnings | ETJ7Z6XBU4 |
| Sandra Plasencia Green Tea Daily SPF 50 Moisturizer | TITANIUM DIOXIDE | Sandra Plasencia Skincare | 43ef1f93-0e89-0a35-e063-6394a90afb51 | 2025-11-19 | Warnings | 15FIX9V2JP |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.