Package 70518-3641-2

Brand: amitriptyline hydrochloride

Generic: amitriptyline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-3641-2
Digits Only 7051836412
Product NDC 70518-3641
Product ID 70518-3641_3c526f1f-9c05-b195-e063-6394a90a53dd
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3641-2)

Marketing

Marketing Status
Marketed Since 2025-08-13
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": "3c526f1f-9c05-b195-e063-6394a90a53dd", "openfda": {"unii": ["26LUD4JO9K"], "rxcui": ["856834"], "spl_set_id": ["c66e9088-4f34-4b97-971e-5272b45cfc97"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3641-2)", "package_ndc": "70518-3641-2", "marketing_start_date": "20250813"}], "brand_name": "Amitriptyline Hydrochloride", "product_id": "70518-3641_3c526f1f-9c05-b195-e063-6394a90a53dd", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "70518-3641", "generic_name": "Amitriptyline Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amitriptyline Hydrochloride", "active_ingredients": [{"name": "AMITRIPTYLINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA214548", "marketing_category": "ANDA", "marketing_start_date": "20230214", "listing_expiration_date": "20261231"}