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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
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| Dolce and Gabbana Everlast Foundation SPF 20 33N Deep | OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDE | Dolce & Gabbana Beauty S.R.L | e249507c-d536-4c1d-a99d-857ca1e833d8 | 2025-08-29 | Warnings | 15FIX9V2JP |
| Dolce and Gabbana Everlast Foundation SPF 20 32W Medium Deep | OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDE | Dolce & Gabbana Beauty S.R.L | ba99edea-bf68-4118-8bb7-ea40322db46a | 2025-08-29 | Warnings | 15FIX9V2JP |
| Dolce and Gabbana Everlast Foundation SPF 20 34W Deep | OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDE | Dolce & Gabbana Beauty S.R.L | 3a239897-9850-417f-8c00-e810a52540c1 | 2025-08-29 | Warnings | 15FIX9V2JP |
| Dolce and Gabbana Everlast Foundation SPF 20 36N Deep | OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDE | Dolce & Gabbana Beauty S.R.L | c495afc3-6486-4652-b743-958f28eccaca | 2025-08-29 | Warnings | 15FIX9V2JP |
| Dolce and Gabbana Everlast Foundation SPF 20 35W Deep | OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDE | Dolce & Gabbana Beauty S.R.L | 5440ed13-b07e-4c81-a407-d9ac68eaa483 | 2025-08-29 | Warnings | 15FIX9V2JP |
| Dolce and Gabbana Everlast Foundation SPF 20 37W Deep | OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDE | Dolce & Gabbana Beauty S.R.L | 9b2c4567-fde7-4b76-9988-b2cba2d3747e | 2025-08-29 | Warnings | 15FIX9V2JP |
| PHOFAY Matte Sunscreen Liquid Foundation SPF 30 2 | ENSULIZOLE,HOMOSALATE,OCTINOXATE,TITANIUM DIOXIDE | Hangzhou Jingshen Trading Co., Ltd. | 3d55291c-9d4c-85c3-e063-6394a90af330 | 2025-08-27 | Warnings | 15FIX9V2JP |
| PHOFAY Matte Sunscreen Liquid Foundation SPF 30 3 | ENSULIZOLE ,HOMOSALATE,OCTINOXATE,TITANIUM DIOXIDE | Hangzhou Jingshen Trading Co., Ltd. | 3d565612-ade5-bfb3-e063-6294a90a0c65 | 2025-08-27 | Warnings | 15FIX9V2JP |
| Sun Bum 30 Mineral Tinted Sunscreen Face | TITANIUM DIOXIDE, ZINC OXIDE | Sun Bum, LLC | 3a290aad-7f40-cb10-e063-6394a90a2e69 | 2025-08-27 | Warnings | 15FIX9V2JP |
| Allergy and Sinus Relief | PELARGONIUM SIDOIDES ROOT, HYDRASTIS CANADENSIS WHOLE, POTASSIUM CHLORIDE, SANGUINARIA CANADENSIS ROOT, PULSATILLA VULGARIS, SILICON DIOXIDE | Schwabe North American, Inc. | c90cc6f5-14ec-41a3-a20a-4e8018bb02fb | 2025-08-25 | Warnings | ETJ7Z6XBU4 |
| PHOFAY Matte Sunscreen Liquid Foundation SPF 30 6 | ENSULIZOLE ,HOMOSALATE ,OCTINOXATE,TITANIUM DIOXIDE | Longway Technology(Guangzhou) Co., Ltd. | 3d0359b6-088f-aa54-e063-6394a90a422f | 2025-08-23 | Warnings | 15FIX9V2JP |
| PHOFAY Matte Sunscreen Liquid Foundation SPF 30 4 | ENSULIZOLE,HOMOSALATE,OCTINOXATE,TITANIUM DIOXIDE | Longway Technology(Guangzhou) Co., Ltd. | 3cdc1ae9-2924-5057-e063-6294a90ad2f3 | 2025-08-21 | Warnings | 15FIX9V2JP |
| PHOFAY Matte Sunscreen Liquid Foundation SPF 30 3 | ENSULIZOLE,HOMOSALATE,OCTINOXATE,TITANIUM DIOXIDE | Longway Technology(Guangzhou) Co., Ltd. | 3b21f1d8-534d-f4ea-e063-6294a90ad2eb | 2025-08-21 | Warnings | 15FIX9V2JP |
| PHOFAY Matte Sunscreen Liquid Foundation SPF 30 5 | ENSULIZOLE,HOMOSALATE,OCTINOXATE,TITANIUM DIOXIDE | Longway Technology(Guangzhou) Co., Ltd. | 3ceb3368-439c-9f6c-e063-6294a90a98ba | 2025-08-21 | Warnings | 15FIX9V2JP |
| PHOFAY Matte Sunscreen Liquid Foundation SPF 30 2 | ENSULIZOLE ,HOMOSALATE ,OCTINOXATE,TITANIUM DIOXIDE | Longway Technology(Guangzhou) Co., Ltd. | 3cc8b151-c07d-7473-e063-6294a90a1cc7 | 2025-08-20 | Warnings | 15FIX9V2JP |
| SEYE | ZINC OXIDE AND TITANIUM DIOXIDE CREAM | Guangzhou Seye Biomedical Technology Co., Ltd. | 3cce91b1-311b-4c95-e063-6294a90a2d7a | 2025-08-20 | Warnings | 15FIX9V2JP |
| Aurum Hypericum | AURUM HYPERICUM | Uriel Pharmacy Inc. | 0c3ed6fe-8dce-0496-e063-6394a90add56 | 2025-08-19 | Warnings | ETJ7Z6XBU4 |
| Fungus Fighter | CANDIDA ALBICANS, SANICULA, TELLURIUM METALLICUM, TORULA CEREVISIAE, ANTIMON. CRUD., ARSENICUM ALB., BARYTA CARB., BRYONIA, CALC. CARB., CARBO VEG., CUPRUM MET., DULCAMARA, GRAPHITES, KALI CARB., LACHESIS, LYCOPODIUM, MEZEREUM, NITRICUM AC., PHOSPHORUS, PHYTOLACCA, SEPIA, SILICEA, SULPHUR, SULPHURICUM AC., ZINC. MET., APIS MEL., THUJA OCC. | Newton Laboratories, Inc. | 93e05175-001b-c639-e053-2a95a90a289c | 2025-08-19 | Warnings | ETJ7Z6XBU4 |
| Fungus Fighter | CANDIDA ALBICANS, SANICULA, TELLURIUM METALLICUM, TORULA CEREVISIAE, ANTIMON. CRUD., ARSENICUM ALB., BARYTA CARB., BRYONIA, CALC. CARB., CARBO VEG., CUPRUM MET., DULCAMARA, GRAPHITES, KALI CARB., LACHESIS, LYCOPODIUM, MEZEREUM, NITRICUM AC., PHOSPHORUS, PHYTOLACCA, SEPIA, SILICEA, SULPHUR, SULPHURICUM AC., ZINC. MET., APIS MEL., THUJA OCC. | Newton Laboratories, Inc. | 9b4276af-b738-3293-e053-2a95a90ad022 | 2025-08-19 | Warnings | ETJ7Z6XBU4 |
| Sun Bum 30 Mineral Sunscreen Face 1.7 OZ | TITANIUM DIOXIDE, ZINC OXIDE | Sun Bum, LLC | 3b1729c5-d8ca-94c7-e063-6394a90a67a5 | 2025-08-18 | Warnings | 15FIX9V2JP |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.