nortriptyline hydrochloride

Generic: nortriptyline hydrochloride

Labeler: taro pharmaceuticals u.s.a., inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name nortriptyline hydrochloride
Generic Name nortriptyline hydrochloride
Labeler taro pharmaceuticals u.s.a., inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

nortriptyline hydrochloride 50 mg/1

Manufacturer
Taro Pharmaceuticals U.S.A., Inc.

Identifiers & Regulatory

Product NDC 51672-4003
Product ID 51672-4003_7ff22c22-51b5-4ce3-93ee-8959359fab3c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075520
Listing Expiration 2026-12-31
Marketing Start 2000-05-08

Pharmacologic Class

Classes
tricyclic antidepressant [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 516724003
Hyphenated Format 51672-4003

Supplemental Identifiers

RxCUI
198045 198046 198047 317136
UPC
0351672400118 0351672400316 0351672400415
UNII
00FN6IH15D

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name nortriptyline hydrochloride (source: ndc)
Generic Name nortriptyline hydrochloride (source: ndc)
Application Number ANDA075520 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 100 CAPSULE in 1 BOTTLE (51672-4003-1)
  • 500 CAPSULE in 1 BOTTLE (51672-4003-2)
  • 90 CAPSULE in 1 BOTTLE (51672-4003-5)
  • 30 CAPSULE in 1 BOTTLE (51672-4003-6)
source: ndc

Packages (4)

51672-4003-1 100 CAPSULE in 1 BOTTLE (51672-4003-1) 51672-4003-2 500 CAPSULE in 1 BOTTLE (51672-4003-2) 51672-4003-5 90 CAPSULE in 1 BOTTLE (51672-4003-5) 51672-4003-6 30 CAPSULE in 1 BOTTLE (51672-4003-6)

Ingredients (1)

nortriptyline hydrochloride (50 mg/1)

Linked Drug Pages (1)

Nortriptyline Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "7ff22c22-51b5-4ce3-93ee-8959359fab3c", "openfda": {"upc": ["0351672400118", "0351672400316", "0351672400415"], "unii": ["00FN6IH15D"], "rxcui": ["198045", "198046", "198047", "317136"], "spl_set_id": ["aee2c1a1-d848-4c3b-8c6d-8a4f6ce94c28"], "manufacturer_name": ["Taro Pharmaceuticals U.S.A., Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (51672-4003-1)", "package_ndc": "51672-4003-1", "marketing_start_date": "20000508"}, {"sample": false, "description": "500 CAPSULE in 1 BOTTLE (51672-4003-2)", "package_ndc": "51672-4003-2", "marketing_start_date": "20000508"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (51672-4003-5)", "package_ndc": "51672-4003-5", "marketing_start_date": "20000508"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE (51672-4003-6)", "package_ndc": "51672-4003-6", "marketing_start_date": "20000508"}], "brand_name": "Nortriptyline Hydrochloride", "product_id": "51672-4003_7ff22c22-51b5-4ce3-93ee-8959359fab3c", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "51672-4003", "generic_name": "Nortriptyline Hydrochloride", "labeler_name": "Taro Pharmaceuticals U.S.A., Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nortriptyline Hydrochloride", "active_ingredients": [{"name": "NORTRIPTYLINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA075520", "marketing_category": "ANDA", "marketing_start_date": "20000508", "listing_expiration_date": "20261231"}