amitriptyline hydrochloride

Generic: amitriptyline hydrochloride

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

Drug Facts

Product Profile

Brand Name amitriptyline hydrochloride
Generic Name amitriptyline hydrochloride
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

amitriptyline hydrochloride 100 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-2374
Product ID 71335-2374_3a62a016-ae4b-4c92-aa9f-eb4f097e2c6c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA217411
Listing Expiration 2026-12-31
Marketing Start 2023-06-10

Pharmacologic Class

Classes
tricyclic antidepressant [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713352374
Hyphenated Format 71335-2374

Supplemental Identifiers

RxCUI
856762
UNII
26LUD4JO9K

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 amitriptyline hydrochloride (source: ndc)
Generic Name amitriptyline hydrochloride (source: ndc)
Application Number ANDA217411 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (71335-2374-1)
  • 60 TABLET in 1 BOTTLE (71335-2374-2)
  • 90 TABLET in 1 BOTTLE (71335-2374-3)
  • 180 TABLET in 1 BOTTLE (71335-2374-4)
  • 28 TABLET in 1 BOTTLE (71335-2374-5)
  • 120 TABLET in 1 BOTTLE (71335-2374-6)
  • 18 TABLET in 1 BOTTLE (71335-2374-7)
  • 8 TABLET in 1 BOTTLE (71335-2374-8)
source: ndc

Packages (8)

Ingredients (1)

amitriptyline hydrochloride (100 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3a62a016-ae4b-4c92-aa9f-eb4f097e2c6c", "openfda": {"unii": ["26LUD4JO9K"], "rxcui": ["856762"], "spl_set_id": ["c707a873-6b67-478f-aa3c-d206a59cbe6d"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-2374-1)", "package_ndc": "71335-2374-1", "marketing_start_date": "20240529"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-2374-2)", "package_ndc": "71335-2374-2", "marketing_start_date": "20240529"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-2374-3)", "package_ndc": "71335-2374-3", "marketing_start_date": "20240529"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE (71335-2374-4)", "package_ndc": "71335-2374-4", "marketing_start_date": "20240529"}, {"sample": false, "description": "28 TABLET in 1 BOTTLE (71335-2374-5)", "package_ndc": "71335-2374-5", "marketing_start_date": "20240529"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (71335-2374-6)", "package_ndc": "71335-2374-6", "marketing_start_date": "20240529"}, {"sample": false, "description": "18 TABLET in 1 BOTTLE (71335-2374-7)", "package_ndc": "71335-2374-7", "marketing_start_date": "20240529"}, {"sample": false, "description": "8 TABLET in 1 BOTTLE (71335-2374-8)", "package_ndc": "71335-2374-8", "marketing_start_date": "20240529"}], "brand_name": "Amitriptyline Hydrochloride", "product_id": "71335-2374_3a62a016-ae4b-4c92-aa9f-eb4f097e2c6c", "dosage_form": "TABLET", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "71335-2374", "generic_name": "Amitriptyline Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amitriptyline Hydrochloride", "active_ingredients": [{"name": "AMITRIPTYLINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA217411", "marketing_category": "ANDA", "marketing_start_date": "20230610", "listing_expiration_date": "20261231"}