Package 72189-581-30

Brand: amitriptyline hcl

Generic: amitriptyline hcl
NDC Package

Package Facts

Identity

Package NDC 72189-581-30
Digits Only 7218958130
Product NDC 72189-581
Description

30 TABLET in 1 BOTTLE (72189-581-30)

Marketing

Marketing Status
Marketed Since 2024-09-19
Brand amitriptyline hcl
Generic amitriptyline hcl
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "227affe9-36ef-2423-e063-6394a90a58f6", "openfda": {"unii": ["26LUD4JO9K"], "rxcui": ["856762"], "spl_set_id": ["227affe9-36ee-2423-e063-6394a90a58f6"], "manufacturer_name": ["Direct_rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72189-581-30)", "package_ndc": "72189-581-30", "marketing_start_date": "20240919"}], "brand_name": "Amitriptyline HCL", "product_id": "72189-581_227affe9-36ef-2423-e063-6394a90a58f6", "dosage_form": "TABLET", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "72189-581", "generic_name": "Amitriptyline HCL", "labeler_name": "Direct_rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amitriptyline HCL", "active_ingredients": [{"name": "AMITRIPTYLINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA217411", "marketing_category": "ANDA", "marketing_start_date": "20240919", "listing_expiration_date": "20261231"}