Package 60760-556-90

Brand: amitriptyline hydrochloride

Generic: amitriptyline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60760-556-90
Digits Only 6076055690
Product NDC 60760-556
Description

90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-556-90)

Marketing

Marketing Status
Marketed Since 2025-05-13
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": "450e40f4-fa23-ad42-e063-6294a90ac458", "openfda": {"unii": ["26LUD4JO9K"], "rxcui": ["856783"], "spl_set_id": ["e3dd745a-57f5-4925-e053-2995a90a43c0"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-556-15)", "package_ndc": "60760-556-15", "marketing_start_date": "20220713"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-556-90)", "package_ndc": "60760-556-90", "marketing_start_date": "20250513"}], "brand_name": "Amitriptyline Hydrochloride", "product_id": "60760-556_450e40f4-fa23-ad42-e063-6294a90ac458", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "60760-556", "generic_name": "Amitriptyline Hydrochloride", "labeler_name": "ST. MARY'S MEDICAL PARK PHARMACY", "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": "20220713", "listing_expiration_date": "20261231"}