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 |
|---|---|---|---|---|---|---|
| RET Heart 7009 | RET HEART | Professional Complementary Health Formulas | e2bf8331-1c50-4216-93a4-1d3cf6404759 | 2026-01-08 | Warnings | ETJ7Z6XBU4 |
| Lumbar Drops 5013 | LUMBAR DROPS | Professional Complementary Health Formulas | ee6b54ea-fb6a-4723-8a0f-970aa82fea80 | 2026-01-08 | Warnings | ETJ7Z6XBU4 |
| Rehydration Drops 2175 | REHYDRATION DROPS | Professional Complementary Health Formulas | 58cc2bd1-c530-43bf-876e-f30d4d95b8da | 2026-01-08 | Warnings | ETJ7Z6XBU4 |
| Dysfunctional Bleeding Drops 2138 | DYSFUNCTIONAL BLEEDING DROPS | Professional Complementary Health Formulas | 3e674c1e-c64b-416d-962f-c03493e80085 | 2026-01-08 | Warnings | ETJ7Z6XBU4 |
| Cervical Drops 5002 | CERVICAL DROPS | Professional Complementary Health Formulas | edd5f196-1423-4d4c-a8c1-89427c4f387e | 2026-01-08 | Warnings | ETJ7Z6XBU4 |
| Asbestox 6005 | ASBESTOX | Professional Complementary Health Formulas | 90bc0d00-01e4-4134-809e-e216fd09852a | 2026-01-08 | Warnings | ETJ7Z6XBU4 |
| H-Clenz Drops 2026 | H-CLENZ DROPS | Professional Complementary Health Formulas | 5dd76d36-e3db-472a-82f8-30643e49eaf7 | 2026-01-08 | Warnings | LMI26O6933 |
| Ledum Combination 9257 | LEDUM COMBINATION | Professional Complementary Health Formulas | 38b89b32-4915-487d-8b2d-250123487b15 | 2026-01-08 | Warnings | ETJ7Z6XBU4 |
| Fourth Chakra (Heart) 7304 | FOURTH CHAKRA (HEART) | Professional Complementary Health Formulas | ef061447-42ae-43d0-b6f3-bf19a96ffe92 | 2026-01-08 | Warnings | ETJ7Z6XBU4 |
| Spinal Drops 5025 | SPINAL DROPS | Professional Complementary Health Formulas | ca6d7250-9c9e-40a6-8d41-88aba33d21dd | 2026-01-08 | Warnings | ETJ7Z6XBU4 |
| Anti-Scar Drops 2084 | ANTI-SCAR DROPS | Professional Complementary Health Formulas | ad0e9159-ed68-48aa-a7d1-7ff5c32ec304 | 2026-01-08 | Warnings | ETJ7Z6XBU4 |
| Fifth Chakra (Throat) 7305 | FIFTH CHAKRA (THROAT) | Professional Complementary Health Formulas | b731f708-10a8-451f-8550-1e7302102b96 | 2026-01-08 | Warnings | ETJ7Z6XBU4 |
| Alumina Combination 9204 | ALUMINA COMBINATION | Professional Complementary Health Formulas | 312cac13-2009-4b8f-a09b-9be2d2801df5 | 2026-01-08 | Warnings | LMI26O6933 |
| Geopathic Stress Drops 2096 | GEOPATHIC STRESS DROPS | Professional Complementary Health Formulas | 7d7302b8-3959-4e1e-ad1f-88d265ba9d32 | 2026-01-08 | Warnings | XM0M87F357 |
| Alopecia Formula 2139 | ALOPECIA FORMULA | Professional Complementary Health Formulas | ce0eaf67-a435-4167-b9ce-c0ff1f8a9dc2 | 2026-01-08 | Warnings | LMI26O6933 |
| Sixth Chakra (Third Eye) 7306 | SIXTH CHAKRA (THIRD EYE) | Professional Complementary Health Formulas | 174024e7-e231-456c-bc00-48a358d7160a | 2026-01-08 | Warnings | ETJ7Z6XBU4 |
| Injury Drops 2034 | INJURY DROPS | Professional Complementary Health Formulas | 024011a0-6471-4016-86d4-19eeb21f0d82 | 2026-01-08 | Warnings | ETJ7Z6XBU4 |
| Colic Drops 2155 | COLIC DROPS | Professional Complementary Health Formulas | 17b9e92f-f4ed-48b4-ab02-8b7cba0a2027 | 2026-01-08 | Warnings | LMI26O6933 |
| Third Chakra (Solar Plexus) 7303 | THIRD CHAKRA (SOLAR PLEXUS) | Professional Complementary Health Formulas | eea89c37-ab87-4cc7-8dfc-e7f42a580dd9 | 2026-01-08 | Warnings | ETJ7Z6XBU4 |
| Nortriptyline Hydrochloride | NORTRIPTYLINE HYDROCHLORIDE | Advagen Pharma Ltd | bef9e24d-e730-4801-ab25-75e7d6bde225 | 2026-01-07 | Boxed warning, Warnings, Adverse reactions | 00FN6IH15D |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.