Package 57237-008-30

Brand: mirtazapine

Generic: mirtazapine
NDC Package

Package Facts

Identity

Package NDC 57237-008-30
Digits Only 5723700830
Product NDC 57237-008
Product ID 57237-008_7616f3f3-c42e-474d-b201-0235120cff36
Description

30 TABLET, FILM COATED in 1 BOTTLE (57237-008-30)

Marketing

Marketing Status
Marketed Since 2004-10-22
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": "7616f3f3-c42e-474d-b201-0235120cff36", "openfda": {"upc": ["0357237007303"], "unii": ["A051Q2099Q"], "rxcui": ["311725", "311726", "314111", "476809"], "spl_set_id": ["58e9b4c6-531f-49c4-a640-6953e70892fe"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (57237-008-05)", "package_ndc": "57237-008-05", "marketing_start_date": "20041022"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (57237-008-30)", "package_ndc": "57237-008-30", "marketing_start_date": "20041022"}], "brand_name": "Mirtazapine", "product_id": "57237-008_7616f3f3-c42e-474d-b201-0235120cff36", "dosage_form": "TABLET, FILM COATED", "product_ndc": "57237-008", "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": "ANDA076921", "marketing_category": "ANDA", "marketing_start_date": "20041022", "listing_expiration_date": "20261231"}