Package 72162-2562-3

Brand: mirtazapine

Generic: mirtazapine
NDC Package

Package Facts

Identity

Package NDC 72162-2562-3
Digits Only 7216225623
Product NDC 72162-2562
Product ID 72162-2562_9fa1cef6-fa23-4cc3-ab32-89951f72b71b
Description

30 TABLET, FILM COATED in 1 BOTTLE (72162-2562-3)

Marketing

Marketing Status
Marketed Since 2025-11-04
Brand mirtazapine
Generic mirtazapine
Sample Package No

Linked Drug Pages (1)

Mirtazapine ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "9fa1cef6-fa23-4cc3-ab32-89951f72b71b", "openfda": {"unii": ["A051Q2099Q"], "rxcui": ["476809"], "spl_set_id": ["55c5905c-6cb8-4ed4-8e69-97f733ca91b5"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72162-2562-3)", "package_ndc": "72162-2562-3", "marketing_start_date": "20251104"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (72162-2562-5)", "package_ndc": "72162-2562-5", "marketing_start_date": "20251104"}], "brand_name": "Mirtazapine", "product_id": "72162-2562_9fa1cef6-fa23-4cc3-ab32-89951f72b71b", "dosage_form": "TABLET, FILM COATED", "product_ndc": "72162-2562", "generic_name": "Mirtazapine", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mirtazapine", "active_ingredients": [{"name": "MIRTAZAPINE", "strength": "7.5 mg/1"}], "application_number": "ANDA076921", "marketing_category": "ANDA", "marketing_start_date": "20090817", "listing_expiration_date": "20261231"}