Package 72189-622-30
Brand: amitriptyline hcl
Generic: amitriptyline hclPackage Facts
Identity
Package NDC
72189-622-30
Digits Only
7218962230
Product NDC
72189-622
Description
30 TABLET, FILM COATED in 1 BOTTLE (72189-622-30)
Marketing
Marketing Status
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": "3504be24-1e76-5e68-e063-6294a90a270a", "openfda": {"unii": ["26LUD4JO9K"], "rxcui": ["856773"], "spl_set_id": ["3504be24-1e75-5e68-e063-6294a90a270a"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72189-622-30)", "package_ndc": "72189-622-30", "marketing_start_date": "20250513"}], "brand_name": "Amitriptyline HCL", "product_id": "72189-622_3504be24-1e76-5e68-e063-6294a90a270a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "72189-622", "generic_name": "Amitriptyline HCL", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amitriptyline HCL", "active_ingredients": [{"name": "AMITRIPTYLINE HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA214548", "marketing_category": "ANDA", "marketing_start_date": "20250513", "listing_expiration_date": "20261231"}