nortriptyline hydrochloride

Generic: nortriptyline hydrochloride

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name nortriptyline hydrochloride
Generic Name nortriptyline hydrochloride
Labeler bryant ranch prepack
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

nortriptyline hydrochloride 50 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-2351
Product ID 71335-2351_ca950abc-d73c-4eec-babf-4c79c8a9defc
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA073556
Listing Expiration 2026-12-31
Marketing Start 2023-11-17

Pharmacologic Class

Classes
tricyclic antidepressant [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713352351
Hyphenated Format 71335-2351

Supplemental Identifiers

RxCUI
198046
UNII
00FN6IH15D

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 ANDA073556 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 30 CAPSULE in 1 BOTTLE, PLASTIC (71335-2351-1)
  • 60 CAPSULE in 1 BOTTLE, PLASTIC (71335-2351-2)
  • 90 CAPSULE in 1 BOTTLE, PLASTIC (71335-2351-3)
  • 28 CAPSULE in 1 BOTTLE, PLASTIC (71335-2351-4)
  • 120 CAPSULE in 1 BOTTLE, PLASTIC (71335-2351-5)
source: ndc

Packages (5)

71335-2351-1 30 CAPSULE in 1 BOTTLE, PLASTIC (71335-2351-1) 71335-2351-2 60 CAPSULE in 1 BOTTLE, PLASTIC (71335-2351-2) 71335-2351-3 90 CAPSULE in 1 BOTTLE, PLASTIC (71335-2351-3) 71335-2351-4 28 CAPSULE in 1 BOTTLE, PLASTIC (71335-2351-4) 71335-2351-5 120 CAPSULE in 1 BOTTLE, PLASTIC (71335-2351-5)

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": "ca950abc-d73c-4eec-babf-4c79c8a9defc", "openfda": {"unii": ["00FN6IH15D"], "rxcui": ["198046"], "spl_set_id": ["4442f029-dd5e-4834-9b01-eb8c638ce4b1"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE, PLASTIC (71335-2351-1)", "package_ndc": "71335-2351-1", "marketing_start_date": "20240221"}, {"sample": false, "description": "60 CAPSULE in 1 BOTTLE, PLASTIC (71335-2351-2)", "package_ndc": "71335-2351-2", "marketing_start_date": "20240221"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE, PLASTIC (71335-2351-3)", "package_ndc": "71335-2351-3", "marketing_start_date": "20240221"}, {"sample": false, "description": "28 CAPSULE in 1 BOTTLE, PLASTIC (71335-2351-4)", "package_ndc": "71335-2351-4", "marketing_start_date": "20240221"}, {"sample": false, "description": "120 CAPSULE in 1 BOTTLE, PLASTIC (71335-2351-5)", "package_ndc": "71335-2351-5", "marketing_start_date": "20240221"}], "brand_name": "Nortriptyline Hydrochloride", "product_id": "71335-2351_ca950abc-d73c-4eec-babf-4c79c8a9defc", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "71335-2351", "generic_name": "Nortriptyline Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nortriptyline Hydrochloride", "active_ingredients": [{"name": "NORTRIPTYLINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA073556", "marketing_category": "ANDA", "marketing_start_date": "20231117", "listing_expiration_date": "20261231"}