Package 60505-0248-1

Brand: mirtazapine

Generic: mirtazapine
NDC Package

Package Facts

Identity

Package NDC 60505-0248-1
Digits Only 6050502481
Product NDC 60505-0248
Description

30 TABLET, FILM COATED in 1 BOTTLE (60505-0248-1)

Marketing

Marketing Status
Marketed Since 2007-08-22
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": "c076cd92-b06d-b317-cc04-6f99b3718cf7", "openfda": {"upc": ["0360505024711", "0360505024810", "0360505024919"], "unii": ["A051Q2099Q"], "rxcui": ["311725", "311726", "314111"], "spl_set_id": ["9675333e-3064-c8cb-a4b4-6c74d9a82f17"], "manufacturer_name": ["Apotex Corp."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (60505-0248-1)", "package_ndc": "60505-0248-1", "marketing_start_date": "20070822"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (60505-0248-3)", "package_ndc": "60505-0248-3", "marketing_start_date": "20070822"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (60505-0248-5)", "package_ndc": "60505-0248-5", "marketing_start_date": "20070822"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (60505-0248-8)", "package_ndc": "60505-0248-8", "marketing_start_date": "20070822"}], "brand_name": "Mirtazapine", "product_id": "60505-0248_c076cd92-b06d-b317-cc04-6f99b3718cf7", "dosage_form": "TABLET, FILM COATED", "product_ndc": "60505-0248", "generic_name": "Mirtazapine", "labeler_name": "Apotex Corp.", "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": "20070822", "listing_expiration_date": "20261231"}