Package 16714-261-01

Brand: amitriptyline hydrochloride

Generic: amitriptyline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 16714-261-01
Digits Only 1671426101
Product NDC 16714-261
Product ID 16714-261_f089e8f9-aed0-4f80-812d-35a969447345
Description

100 TABLET, FILM COATED in 1 BOTTLE (16714-261-01)

Marketing

Marketing Status
Marketed Since 2021-08-25
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": "f089e8f9-aed0-4f80-812d-35a969447345", "openfda": {"unii": ["26LUD4JO9K"], "rxcui": ["856762", "856773", "856783", "856834", "856845", "856853"], "spl_set_id": ["8ed28f42-e41a-45ca-a86f-849ebeb6ab80"], "manufacturer_name": ["Northstar Rx LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (16714-261-01)", "package_ndc": "16714-261-01", "marketing_start_date": "20210825"}], "brand_name": "Amitriptyline Hydrochloride", "product_id": "16714-261_f089e8f9-aed0-4f80-812d-35a969447345", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "16714-261", "generic_name": "Amitriptyline Hydrochloride", "labeler_name": "Northstar Rx LLC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amitriptyline Hydrochloride", "active_ingredients": [{"name": "AMITRIPTYLINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA210086", "marketing_category": "ANDA", "marketing_start_date": "20210825", "listing_expiration_date": "20261231"}