Package 72888-068-01

Brand: amitriptyline hydrochloride

Generic: amitriptyline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72888-068-01
Digits Only 7288806801
Product NDC 72888-068
Description

100 TABLET, FILM COATED in 1 BOTTLE (72888-068-01)

Marketing

Marketing Status
Marketed Since 2023-05-01
Brand amitriptyline hydrochloride
Generic amitriptyline hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "451e8ad6-a78e-429b-e063-6394a90a2bdb", "openfda": {"upc": ["0372888067001", "0372888072012", "0372888071015", "0372888070018", "0372888067018", "0372888069012", "0372888071039", "0372888069005", "0372888068008"], "unii": ["26LUD4JO9K"], "rxcui": ["856762", "856773", "856783", "856834", "856845", "856853"], "spl_set_id": ["651bd090-a420-4dd8-89b0-4cb766c144c2"], "manufacturer_name": ["Advagen Pharma Ltd"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (72888-068-00)", "package_ndc": "72888-068-00", "marketing_start_date": "20230501"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (72888-068-01)", "package_ndc": "72888-068-01", "marketing_start_date": "20230501"}], "brand_name": "Amitriptyline Hydrochloride", "product_id": "72888-068_451e8ad6-a78e-429b-e063-6394a90a2bdb", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "72888-068", "generic_name": "Amitriptyline Hydrochloride", "labeler_name": "Advagen Pharma Ltd", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amitriptyline Hydrochloride", "active_ingredients": [{"name": "AMITRIPTYLINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA215376", "marketing_category": "ANDA", "marketing_start_date": "20230501", "listing_expiration_date": "20261231"}