Package 72189-444-30

Brand: amitriptyline hcl

Generic: amitriptyline hcl
NDC Package

Package Facts

Identity

Package NDC 72189-444-30
Digits Only 7218944430
Product NDC 72189-444
Description

30 TABLET, FILM COATED in 1 BOTTLE (72189-444-30)

Marketing

Marketing Status
Marketed Since 2023-03-14
Brand amitriptyline hcl
Generic amitriptyline hcl
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2c4d9d53-d060-978d-e063-6294a90ac22d", "openfda": {"unii": ["26LUD4JO9K"], "rxcui": ["856853"], "spl_set_id": ["f6dc463b-3601-48c0-e053-6294a90a2d77"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72189-444-30)", "package_ndc": "72189-444-30", "marketing_start_date": "20230314"}], "brand_name": "Amitriptyline HCL", "product_id": "72189-444_2c4d9d53-d060-978d-e063-6294a90ac22d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "72189-444", "generic_name": "Amitriptyline HCL", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amitriptyline HCL", "active_ingredients": [{"name": "AMITRIPTYLINE HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA214548", "marketing_category": "ANDA", "marketing_start_date": "20230314", "listing_expiration_date": "20261231"}