Package 70518-4366-0

Brand: amitriptyline hydrochloride

Generic: amitriptyline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-4366-0
Digits Only 7051843660
Product NDC 70518-4366
Product ID 70518-4366_40319bfe-94c8-50ec-e063-6394a90a2912
Description

90 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-4366-0)

Marketing

Marketing Status
Marketed Since 2025-06-19
Brand amitriptyline hydrochloride
Generic amitriptyline hydrochloride
Sample Package No

Linked Drug Pages (0)

No linked drugs yet.

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "40319bfe-94c8-50ec-e063-6394a90a2912", "openfda": {"unii": ["26LUD4JO9K"], "rxcui": ["856762"], "spl_set_id": ["61b29703-cfc2-45c7-ae24-7bf3b77e8587"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-4366-0)", "package_ndc": "70518-4366-0", "marketing_start_date": "20250619"}], "brand_name": "Amitriptyline Hydrochloride", "product_id": "70518-4366_40319bfe-94c8-50ec-e063-6394a90a2912", "dosage_form": "TABLET, COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "70518-4366", "generic_name": "Amitriptyline Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amitriptyline Hydrochloride", "active_ingredients": [{"name": "AMITRIPTYLINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA212654", "marketing_category": "ANDA", "marketing_start_date": "20250619", "listing_expiration_date": "20261231"}