amitriptyline hcl

Generic: amitriptyline hcl

Labeler: direct_rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name amitriptyline hcl
Generic Name amitriptyline hcl
Labeler direct_rx
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

amitriptyline hydrochloride 150 mg/1

Manufacturer
Direct_Rx

Identifiers & Regulatory

Product NDC 72189-588
Product ID 72189-588_23ab2afe-06c2-fa61-e063-6394a90abcf8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA213999
Listing Expiration 2026-12-31
Marketing Start 2024-10-04

Pharmacologic Class

Classes
tricyclic antidepressant [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72189588
Hyphenated Format 72189-588

Supplemental Identifiers

RxCUI
856773
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 hcl (source: ndc)
Generic Name amitriptyline hcl (source: ndc)
Application Number ANDA213999 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 150 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (72189-588-30)
source: ndc

Packages (1)

72189-588-30 30 TABLET, FILM COATED in 1 BOTTLE (72189-588-30)

Ingredients (1)

amitriptyline hydrochloride (150 mg/1)

Linked Drug Pages (1)

Amitriptyline HCL ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "23ab2afe-06c2-fa61-e063-6394a90abcf8", "openfda": {"unii": ["26LUD4JO9K"], "rxcui": ["856773"], "spl_set_id": ["23ab2afe-06c1-fa61-e063-6394a90abcf8"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72189-588-30)", "package_ndc": "72189-588-30", "marketing_start_date": "20241004"}], "brand_name": "Amitriptyline HCL", "product_id": "72189-588_23ab2afe-06c2-fa61-e063-6394a90abcf8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "72189-588", "generic_name": "Amitriptyline HCL", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amitriptyline HCL", "active_ingredients": [{"name": "AMITRIPTYLINE HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA213999", "marketing_category": "ANDA", "marketing_start_date": "20241004", "listing_expiration_date": "20261231"}