Package 82868-093-90

Brand: amitriptyline hydrochloride

Generic: amitriptyline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 82868-093-90
Digits Only 8286809390
Product NDC 82868-093
Product ID 82868-093_471b99ea-825a-309f-e063-6394a90a305f
Description

90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82868-093-90)

Marketing

Marketing Status
Marketed Since 2025-11-26
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": "471b99ea-825a-309f-e063-6394a90a305f", "openfda": {"unii": ["26LUD4JO9K"], "rxcui": ["856783"], "spl_set_id": ["471b99ac-395c-3137-e063-6394a90af18d"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82868-093-90)", "package_ndc": "82868-093-90", "marketing_start_date": "20251126"}], "brand_name": "Amitriptyline Hydrochloride", "product_id": "82868-093_471b99ea-825a-309f-e063-6394a90a305f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "82868-093", "generic_name": "Amitriptyline Hydrochloride", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amitriptyline Hydrochloride", "active_ingredients": [{"name": "AMITRIPTYLINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA214548", "marketing_category": "ANDA", "marketing_start_date": "20251126", "listing_expiration_date": "20261231"}