Package 60760-685-90

Brand: amitriptyline hydrochloride

Generic: amitriptyline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60760-685-90
Digits Only 6076068590
Product NDC 60760-685
Product ID 60760-685_35a6fab2-4bf5-22e1-e063-6394a90afe12
Description

90 TABLET in 1 BOTTLE, PLASTIC (60760-685-90)

Marketing

Marketing Status
Marketed Since 2025-05-13
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": "35a6fab2-4bf5-22e1-e063-6394a90afe12", "openfda": {"unii": ["26LUD4JO9K"], "rxcui": ["856834"], "spl_set_id": ["35a6e911-507a-ef0d-e063-6294a90a07e1"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (60760-685-90)", "package_ndc": "60760-685-90", "marketing_start_date": "20250513"}], "brand_name": "Amitriptyline Hydrochloride", "product_id": "60760-685_35a6fab2-4bf5-22e1-e063-6394a90afe12", "dosage_form": "TABLET", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "60760-685", "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": "25 mg/1"}], "application_number": "ANDA217411", "marketing_category": "ANDA", "marketing_start_date": "20230610", "listing_expiration_date": "20261231"}