Package 82868-075-30

Brand: amitriptyline hydrochloride

Generic: amitriptyline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 82868-075-30
Digits Only 8286807530
Product NDC 82868-075
Product ID 82868-075_476b3f59-b789-16bf-e063-6394a90a04cf
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82868-075-30)

Marketing

Marketing Status
Marketed Since 2025-06-11
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": "476b3f59-b789-16bf-e063-6394a90a04cf", "openfda": {"unii": ["26LUD4JO9K"], "rxcui": ["856834"], "spl_set_id": ["43450e62-d8c1-b39e-e063-6294a90a42ee"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82868-075-30)", "package_ndc": "82868-075-30", "marketing_start_date": "20250611"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82868-075-90)", "package_ndc": "82868-075-90", "marketing_start_date": "20250326"}], "brand_name": "Amitriptyline Hydrochloride", "product_id": "82868-075_476b3f59-b789-16bf-e063-6394a90a04cf", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "82868-075", "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": "25 mg/1"}], "application_number": "ANDA214548", "marketing_category": "ANDA", "marketing_start_date": "20250326", "listing_expiration_date": "20271231"}