Package 50090-3564-2

Brand: amitriptyline hydrochloride

Generic: amitriptyline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-3564-2
Digits Only 5009035642
Product NDC 50090-3564
Description

60 TABLET, FILM COATED in 1 BOTTLE (50090-3564-2)

Marketing

Marketing Status
Marketed Since 2018-08-30
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": "f4f09800-e299-40ce-8637-9180a886de99", "openfda": {"unii": ["26LUD4JO9K"], "rxcui": ["856762"], "spl_set_id": ["9440dd10-2f0d-42a7-a037-3ab8729708f6"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (50090-3564-2)", "package_ndc": "50090-3564-2", "marketing_start_date": "20180830"}], "brand_name": "AMITRIPTYLINE HYDROCHLORIDE", "product_id": "50090-3564_f4f09800-e299-40ce-8637-9180a886de99", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "50090-3564", "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": "ANDA202446", "marketing_category": "ANDA", "marketing_start_date": "20141205", "listing_expiration_date": "20261231"}