Package 72189-626-30

Brand: mirtazapine

Generic: mirtazapine
NDC Package

Package Facts

Identity

Package NDC 72189-626-30
Digits Only 7218962630
Product NDC 72189-626
Product ID 72189-626_3699b988-6d9b-dcc1-e063-6394a90ab38d
Description

30 TABLET, FILM COATED in 1 BOTTLE (72189-626-30)

Marketing

Marketing Status
Marketed Since 2025-06-02
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": "3699b988-6d9b-dcc1-e063-6394a90ab38d", "openfda": {"unii": ["A051Q2099Q"], "rxcui": ["314111"], "spl_set_id": ["3699b988-6d9a-dcc1-e063-6394a90ab38d"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72189-626-30)", "package_ndc": "72189-626-30", "marketing_start_date": "20250602"}], "brand_name": "Mirtazapine", "product_id": "72189-626_3699b988-6d9b-dcc1-e063-6394a90ab38d", "dosage_form": "TABLET, FILM COATED", "product_ndc": "72189-626", "generic_name": "Mirtazapine", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mirtazapine", "active_ingredients": [{"name": "MIRTAZAPINE", "strength": "30 mg/1"}], "application_number": "ANDA076921", "marketing_category": "ANDA", "marketing_start_date": "20250602", "listing_expiration_date": "20261231"}