Package 70518-3979-0

Brand: amitriptyline hydrochloride

Generic: amitriptyline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-3979-0
Digits Only 7051839790
Product NDC 70518-3979
Product ID 70518-3979_3bc7a9dc-12b5-32dc-e063-6294a90a1afc
Description

90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3979-0)

Marketing

Marketing Status
Marketed Since 2024-01-10
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": "3bc7a9dc-12b5-32dc-e063-6294a90a1afc", "openfda": {"unii": ["26LUD4JO9K"], "rxcui": ["856853"], "spl_set_id": ["9ced0126-d597-48fb-96d3-577333760048"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3979-0)", "package_ndc": "70518-3979-0", "marketing_start_date": "20240110"}], "brand_name": "Amitriptyline Hydrochloride", "product_id": "70518-3979_3bc7a9dc-12b5-32dc-e063-6294a90a1afc", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "70518-3979", "generic_name": "Amitriptyline Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amitriptyline Hydrochloride", "active_ingredients": [{"name": "AMITRIPTYLINE HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA214548", "marketing_category": "ANDA", "marketing_start_date": "20240110", "listing_expiration_date": "20261231"}