Package 80425-0362-1

Brand: amitriptyline hydrochloride

Generic: amitriptyline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 80425-0362-1
Digits Only 8042503621
Product NDC 80425-0362
Product ID 80425-0362_2a994e77-4ae5-1307-e063-6394a90a5bd3
Description

30 TABLET, FILM COATED in 1 BOTTLE (80425-0362-1)

Marketing

Marketing Status
Marketed Since 2023-10-20
Brand amitriptyline hydrochloride
Generic amitriptyline hydrochloride
Sample Package No

Linked Drug Pages (1)

Amitriptyline Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2a994e77-4ae5-1307-e063-6394a90a5bd3", "openfda": {"unii": ["26LUD4JO9K"], "rxcui": ["856845"], "spl_set_id": ["082b620f-8085-d205-e063-6294a90ac6de"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (80425-0362-1)", "package_ndc": "80425-0362-1", "marketing_start_date": "20231020"}], "brand_name": "Amitriptyline Hydrochloride", "product_id": "80425-0362_2a994e77-4ae5-1307-e063-6394a90a5bd3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "80425-0362", "generic_name": "Amitriptyline Hydrochloride", "labeler_name": "Advanced Rx of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amitriptyline Hydrochloride", "active_ingredients": [{"name": "AMITRIPTYLINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA214548", "marketing_category": "ANDA", "marketing_start_date": "20231020", "listing_expiration_date": "20261231"}