Package 51655-632-26

Brand: amitriptyline hydrochloride

Generic: amitriptyline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51655-632-26
Digits Only 5165563226
Product NDC 51655-632
Product ID 51655-632_494f537b-78b7-4502-e063-6294a90a3092
Description

90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-632-26)

Marketing

Marketing Status
Marketed Since 2022-06-02
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": "494f537b-78b7-4502-e063-6294a90a3092", "openfda": {"unii": ["26LUD4JO9K"], "rxcui": ["856783"], "spl_set_id": ["e3afe026-7072-0a7d-e053-2995a90a52d4"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-632-26)", "package_ndc": "51655-632-26", "marketing_start_date": "20220602"}], "brand_name": "AMITRIPTYLINE HYDROCHLORIDE", "product_id": "51655-632_494f537b-78b7-4502-e063-6294a90a3092", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "51655-632", "generic_name": "AMITRIPTYLINE HYDROCHLORIDE", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "AMITRIPTYLINE HYDROCHLORIDE", "active_ingredients": [{"name": "AMITRIPTYLINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA202446", "marketing_category": "ANDA", "marketing_start_date": "20220602", "listing_expiration_date": "20271231"}