Package 70518-4054-1

Brand: amitriptyline hydrochloride

Generic: amitriptyline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-4054-1
Digits Only 7051840541
Product NDC 70518-4054
Product ID 70518-4054_3fa22a4c-ca56-2a09-e063-6294a90ac89a
Description

30 TABLET in 1 BLISTER PACK (70518-4054-1)

Marketing

Marketing Status
Marketed Since 2024-05-06
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": "3fa22a4c-ca56-2a09-e063-6294a90ac89a", "openfda": {"unii": ["26LUD4JO9K"], "rxcui": ["856762"], "spl_set_id": ["bb02d7b8-8f1a-4cc4-b763-223e6894f02c"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-4054-1)", "package_ndc": "70518-4054-1", "marketing_start_date": "20240506"}], "brand_name": "Amitriptyline Hydrochloride", "product_id": "70518-4054_3fa22a4c-ca56-2a09-e063-6294a90ac89a", "dosage_form": "TABLET", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "70518-4054", "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": "ANDA217411", "marketing_category": "ANDA", "marketing_start_date": "20240417", "listing_expiration_date": "20261231"}