Package 57237-011-06

Brand: mirtazapine

Generic: mirtazapine
NDC Package

Package Facts

Identity

Package NDC 57237-011-06
Digits Only 5723701106
Product NDC 57237-011
Description

5 BLISTER PACK in 1 CARTON (57237-011-06) / 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2005-12-08
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": "ed2cd1df-697f-4e63-8097-7802be5eb6bb", "openfda": {"unii": ["A051Q2099Q"], "rxcui": ["283406", "283407", "283485"], "spl_set_id": ["73b7bbd9-7dba-4559-890f-3f8dd821e215"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "5 BLISTER PACK in 1 CARTON (57237-011-06)  / 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK", "package_ndc": "57237-011-06", "marketing_start_date": "20051208"}], "brand_name": "Mirtazapine", "product_id": "57237-011_ed2cd1df-697f-4e63-8097-7802be5eb6bb", "dosage_form": "TABLET, ORALLY DISINTEGRATING", "product_ndc": "57237-011", "generic_name": "Mirtazapine", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mirtazapine", "active_ingredients": [{"name": "MIRTAZAPINE", "strength": "15 mg/1"}], "application_number": "ANDA077376", "marketing_category": "ANDA", "marketing_start_date": "20051208", "listing_expiration_date": "20261231"}