Package 60760-732-90

Brand: amitriptyline hydrochloride

Generic: amitriptyline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60760-732-90
Digits Only 6076073290
Product NDC 60760-732
Product ID 60760-732_485b7f90-31f1-0f8d-e063-6294a90a4866
Description

90 TABLET in 1 BOTTLE, PLASTIC (60760-732-90)

Marketing

Marketing Status
Marketed Since 2026-01-14
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": "485b7f90-31f1-0f8d-e063-6294a90a4866", "openfda": {"unii": ["26LUD4JO9K"], "rxcui": ["856762"], "spl_set_id": ["485b87c3-2a51-133b-e063-6294a90a95c3"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (60760-732-90)", "package_ndc": "60760-732-90", "marketing_start_date": "20260114"}], "brand_name": "Amitriptyline Hydrochloride", "product_id": "60760-732_485b7f90-31f1-0f8d-e063-6294a90a4866", "dosage_form": "TABLET", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "60760-732", "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": "ANDA217411", "marketing_category": "ANDA", "marketing_start_date": "20230610", "listing_expiration_date": "20271231"}