Package 82804-092-30

Brand: amitriptyline hydrochloride

Generic: amitriptyline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 82804-092-30
Digits Only 8280409230
Product NDC 82804-092
Product ID 82804-092_61133866-b01c-4278-93fb-4564c1b56e54
Description

30 TABLET, FILM COATED in 1 BOTTLE (82804-092-30)

Marketing

Marketing Status
Marketed Since 2024-03-29
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": "61133866-b01c-4278-93fb-4564c1b56e54", "openfda": {"upc": ["0382804092307"], "unii": ["26LUD4JO9K"], "rxcui": ["856783"], "spl_set_id": ["61133866-b01c-4278-93fb-4564c1b56e54"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (82804-092-30)", "package_ndc": "82804-092-30", "marketing_start_date": "20240329"}], "brand_name": "Amitriptyline Hydrochloride", "product_id": "82804-092_61133866-b01c-4278-93fb-4564c1b56e54", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "82804-092", "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": "10 mg/1"}], "application_number": "ANDA214548", "marketing_category": "ANDA", "marketing_start_date": "20210526", "listing_expiration_date": "20261231"}