Package 50090-6418-2

Brand: amitriptyline hydrochloride

Generic: amitriptyline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-6418-2
Digits Only 5009064182
Product NDC 50090-6418
Description

60 TABLET, FILM COATED in 1 BOTTLE (50090-6418-2)

Marketing

Marketing Status
Marketed Since 2023-03-31
Brand amitriptyline hydrochloride
Generic amitriptyline hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "db7d6cf0-2227-4560-b9e7-16da4845c354", "openfda": {"unii": ["26LUD4JO9K"], "rxcui": ["856762"], "spl_set_id": ["1a622039-0a79-407c-8f15-2ea0c5844136"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (50090-6418-2)", "package_ndc": "50090-6418-2", "marketing_start_date": "20230331"}], "brand_name": "Amitriptyline Hydrochloride", "product_id": "50090-6418_db7d6cf0-2227-4560-b9e7-16da4845c354", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "50090-6418", "generic_name": "Amitriptyline Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amitriptyline Hydrochloride", "active_ingredients": [{"name": "AMITRIPTYLINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA214548", "marketing_category": "ANDA", "marketing_start_date": "20210526", "listing_expiration_date": "20261231"}