Package 72603-558-02

Brand: mirtazapine

Generic: mirtazapine
NDC Package

Package Facts

Identity

Package NDC 72603-558-02
Digits Only 7260355802
Product NDC 72603-558
Product ID 72603-558_979eec8b-1bf4-466b-812e-85a111ce1cb5
Description

500 TABLET, FILM COATED in 1 BOTTLE (72603-558-02)

Marketing

Marketing Status
Marketed Since 2025-04-01
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": "979eec8b-1bf4-466b-812e-85a111ce1cb5", "openfda": {"upc": ["0372603558012"], "unii": ["A051Q2099Q"], "rxcui": ["476809"], "spl_set_id": ["979eec8b-1bf4-466b-812e-85a111ce1cb5"], "manufacturer_name": ["NorthStar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72603-558-01)", "package_ndc": "72603-558-01", "marketing_start_date": "20250401"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (72603-558-02)", "package_ndc": "72603-558-02", "marketing_start_date": "20250401"}], "brand_name": "Mirtazapine", "product_id": "72603-558_979eec8b-1bf4-466b-812e-85a111ce1cb5", "dosage_form": "TABLET, FILM COATED", "product_ndc": "72603-558", "generic_name": "Mirtazapine", "labeler_name": "NorthStar Rx LLC", "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": "20250401", "listing_expiration_date": "20261231"}