Package 60760-907-90

Brand: amitriptyline hydrochloride

Generic: amitriptyline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60760-907-90
Digits Only 6076090790
Product NDC 60760-907
Product ID 60760-907_1b2d3cb4-67e3-3e2d-e063-6394a90aa43f
Description

90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-907-90)

Marketing

Marketing Status
Marketed Since 2024-06-12
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": "1b2d3cb4-67e3-3e2d-e063-6394a90aa43f", "openfda": {"unii": ["26LUD4JO9K"], "rxcui": ["856762"], "spl_set_id": ["1b2d2bb8-78c8-7e8e-e063-6294a90a2576"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-907-90)", "package_ndc": "60760-907-90", "marketing_start_date": "20240612"}], "brand_name": "Amitriptyline Hydrochloride", "product_id": "60760-907_1b2d3cb4-67e3-3e2d-e063-6394a90aa43f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "60760-907", "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": "100 mg/1"}], "application_number": "ANDA214548", "marketing_category": "ANDA", "marketing_start_date": "20210526", "listing_expiration_date": "20261231"}