Package 70518-3654-2

Brand: amitriptyline hydrochloride

Generic: amitriptyline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-3654-2
Digits Only 7051836542
Product NDC 70518-3654
Product ID 70518-3654_3f2766be-8ff5-afb2-e063-6394a90a65a4
Description

90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3654-2)

Marketing

Marketing Status
Marketed Since 2024-10-10
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": "3f2766be-8ff5-afb2-e063-6394a90a65a4", "openfda": {"unii": ["26LUD4JO9K"], "rxcui": ["856845"], "spl_set_id": ["2becb369-62db-4763-b0e5-0c8bbaa44418"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3654-2)", "package_ndc": "70518-3654-2", "marketing_start_date": "20241010"}], "brand_name": "Amitriptyline Hydrochloride", "product_id": "70518-3654_3f2766be-8ff5-afb2-e063-6394a90a65a4", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "70518-3654", "generic_name": "Amitriptyline Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amitriptyline Hydrochloride", "active_ingredients": [{"name": "AMITRIPTYLINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA214548", "marketing_category": "ANDA", "marketing_start_date": "20230220", "listing_expiration_date": "20261231"}