Package 82804-100-30

Brand: amitriptyline hydrochloride

Generic: amitriptyline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 82804-100-30
Digits Only 8280410030
Product NDC 82804-100
Product ID 82804-100_ce665435-b2f1-4fcd-ae20-4f372f376095
Description

30 TABLET, FILM COATED in 1 BOTTLE (82804-100-30)

Marketing

Marketing Status
Marketed Since 2024-05-01
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": "ce665435-b2f1-4fcd-ae20-4f372f376095", "openfda": {"upc": ["0382804100309"], "unii": ["26LUD4JO9K"], "rxcui": ["856834"], "spl_set_id": ["ce665435-b2f1-4fcd-ae20-4f372f376095"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (82804-100-30)", "package_ndc": "82804-100-30", "marketing_start_date": "20240501"}], "brand_name": "Amitriptyline Hydrochloride", "product_id": "82804-100_ce665435-b2f1-4fcd-ae20-4f372f376095", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "82804-100", "generic_name": "Amitriptyline Hydrochloride", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amitriptyline Hydrochloride", "active_ingredients": [{"name": "AMITRIPTYLINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA214548", "marketing_category": "ANDA", "marketing_start_date": "20210526", "listing_expiration_date": "20261231"}