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, FILM COATED
Routes
ORAL
Active Ingredients

amitriptyline hydrochloride 150 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-0566
Product ID 71335-0566_40f41ec8-0357-4851-82f1-0a94ee15a24a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202446
Listing Expiration 2026-12-31
Marketing Start 2014-12-26

Pharmacologic Class

Classes
tricyclic antidepressant [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713350566
Hyphenated Format 71335-0566

Supplemental Identifiers

RxCUI
856762 856773 856783 856834 856845 856853
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 ANDA202446 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 150 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (71335-0566-1)
  • 120 TABLET, FILM COATED in 1 BOTTLE (71335-0566-2)
  • 60 TABLET, FILM COATED in 1 BOTTLE (71335-0566-3)
  • 90 TABLET, FILM COATED in 1 BOTTLE (71335-0566-4)
  • 18 TABLET, FILM COATED in 1 BOTTLE (71335-0566-5)
source: ndc

Packages (5)

71335-0566-1 30 TABLET, FILM COATED in 1 BOTTLE (71335-0566-1) 71335-0566-2 120 TABLET, FILM COATED in 1 BOTTLE (71335-0566-2) 71335-0566-3 60 TABLET, FILM COATED in 1 BOTTLE (71335-0566-3) 71335-0566-4 90 TABLET, FILM COATED in 1 BOTTLE (71335-0566-4) 71335-0566-5 18 TABLET, FILM COATED in 1 BOTTLE (71335-0566-5)

Ingredients (1)

amitriptyline hydrochloride (150 mg/1)

Linked Drug Pages (1)

AMITRIPTYLINE HYDROCHLORIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "40f41ec8-0357-4851-82f1-0a94ee15a24a", "openfda": {"unii": ["26LUD4JO9K"], "rxcui": ["856762", "856773", "856783", "856834", "856845", "856853"], "spl_set_id": ["76d3f4fd-4603-4cfc-94ab-2e62c0bdae75"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-0566-1)", "package_ndc": "71335-0566-1", "marketing_start_date": "20150921"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (71335-0566-2)", "package_ndc": "71335-0566-2", "marketing_start_date": "20150921"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-0566-3)", "package_ndc": "71335-0566-3", "marketing_start_date": "20150921"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-0566-4)", "package_ndc": "71335-0566-4", "marketing_start_date": "20150921"}, {"sample": false, "description": "18 TABLET, FILM COATED in 1 BOTTLE (71335-0566-5)", "package_ndc": "71335-0566-5", "marketing_start_date": "20150921"}], "brand_name": "AMITRIPTYLINE HYDROCHLORIDE", "product_id": "71335-0566_40f41ec8-0357-4851-82f1-0a94ee15a24a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "71335-0566", "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": "150 mg/1"}], "application_number": "ANDA202446", "marketing_category": "ANDA", "marketing_start_date": "20141226", "listing_expiration_date": "20261231"}