Package 42291-952-50

Brand: mirtazapine

Generic: mirtazapine
NDC Package

Package Facts

Identity

Package NDC 42291-952-50
Digits Only 4229195250
Product NDC 42291-952
Description

500 TABLET, FILM COATED in 1 BOTTLE (42291-952-50)

Marketing

Marketing Status
Marketed Since 2025-05-20
Brand mirtazapine
Generic mirtazapine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "35923954-c6ec-3d84-e063-6394a90aecf4", "openfda": {"upc": ["0342291952508"], "unii": ["A051Q2099Q"], "rxcui": ["314111"], "spl_set_id": ["35922615-7619-3852-e063-6394a90a2e55"], "manufacturer_name": ["AvKARE"]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (42291-952-50)", "package_ndc": "42291-952-50", "marketing_start_date": "20250520"}], "brand_name": "Mirtazapine", "product_id": "42291-952_35923954-c6ec-3d84-e063-6394a90aecf4", "dosage_form": "TABLET, FILM COATED", "product_ndc": "42291-952", "generic_name": "Mirtazapine", "labeler_name": "AvKARE", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mirtazapine", "active_ingredients": [{"name": "MIRTAZAPINE", "strength": "30 mg/1"}], "application_number": "ANDA077666", "marketing_category": "ANDA", "marketing_start_date": "20250520", "listing_expiration_date": "20261231"}