Package 70518-3621-1

Brand: amitriptyline hydrochloride

Generic: amitriptyline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-3621-1
Digits Only 7051836211
Product NDC 70518-3621
Description

90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3621-1)

Marketing

Marketing Status
Marketed Since 2023-01-28
Brand amitriptyline hydrochloride
Generic amitriptyline hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3f18ad0d-ede1-76d9-e063-6394a90a1ef5", "openfda": {"unii": ["26LUD4JO9K"], "rxcui": ["856783"], "spl_set_id": ["abf6a3f5-0df9-4b23-995d-63b973ef80c1"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3621-0)", "package_ndc": "70518-3621-0", "marketing_start_date": "20230125"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3621-1)", "package_ndc": "70518-3621-1", "marketing_start_date": "20230128"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3621-2)", "package_ndc": "70518-3621-2", "marketing_start_date": "20230505"}], "brand_name": "Amitriptyline Hydrochloride", "product_id": "70518-3621_3f18ad0d-ede1-76d9-e063-6394a90a1ef5", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "70518-3621", "generic_name": "Amitriptyline Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amitriptyline Hydrochloride", "active_ingredients": [{"name": "AMITRIPTYLINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA214548", "marketing_category": "ANDA", "marketing_start_date": "20230125", "listing_expiration_date": "20261231"}