Package 13107-001-90

Brand: mirtazapine

Generic: mirtazapine
NDC Package

Package Facts

Identity

Package NDC 13107-001-90
Digits Only 1310700190
Product NDC 13107-001
Description

90 TABLET, FILM COATED in 1 BOTTLE (13107-001-90)

Marketing

Marketing Status
Marketed Since 2009-08-17
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": "4329eeed-8071-4b6c-887d-0cd00647b84c", "openfda": {"unii": ["A051Q2099Q"], "rxcui": ["311725", "311726", "314111", "476809"], "spl_set_id": ["aa05d606-29fd-443e-802b-1d65584d6bb1"], "manufacturer_name": ["Aurolife Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (13107-001-01)", "package_ndc": "13107-001-01", "marketing_start_date": "20090817"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (13107-001-05)", "package_ndc": "13107-001-05", "marketing_start_date": "20090817"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (13107-001-30)", "package_ndc": "13107-001-30", "marketing_start_date": "20090817"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (13107-001-60)", "package_ndc": "13107-001-60", "marketing_start_date": "20090817"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (13107-001-90)", "package_ndc": "13107-001-90", "marketing_start_date": "20090817"}], "brand_name": "Mirtazapine", "product_id": "13107-001_4329eeed-8071-4b6c-887d-0cd00647b84c", "dosage_form": "TABLET, FILM COATED", "product_ndc": "13107-001", "generic_name": "Mirtazapine", "labeler_name": "Aurolife Pharma LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mirtazapine", "active_ingredients": [{"name": "MIRTAZAPINE", "strength": "7.5 mg/1"}], "application_number": "ANDA076921", "marketing_category": "ANDA", "marketing_start_date": "20090817", "listing_expiration_date": "20261231"}