Package 50090-2140-0

Brand: mirtazapine

Generic: mirtazapine
NDC Package

Package Facts

Identity

Package NDC 50090-2140-0
Digits Only 5009021400
Product NDC 50090-2140
Product ID 50090-2140_a6586ed3-0ef9-44a9-b32d-9232dd5f964e
Description

30 TABLET, FILM COATED in 1 BOTTLE (50090-2140-0)

Marketing

Marketing Status
Marketed Since 2015-10-19
Brand mirtazapine
Generic mirtazapine
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "a6586ed3-0ef9-44a9-b32d-9232dd5f964e", "openfda": {"unii": ["A051Q2099Q"], "rxcui": ["311725", "314111"], "spl_set_id": ["67e753ad-9919-416b-9e8f-aab0fa808066"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-2140-0)", "package_ndc": "50090-2140-0", "marketing_start_date": "20151019"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-2140-1)", "package_ndc": "50090-2140-1", "marketing_start_date": "20151019"}], "brand_name": "Mirtazapine", "product_id": "50090-2140_a6586ed3-0ef9-44a9-b32d-9232dd5f964e", "dosage_form": "TABLET, FILM COATED", "product_ndc": "50090-2140", "generic_name": "Mirtazapine", "labeler_name": "A-S Medication Solutions", "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": "20090817", "listing_expiration_date": "20271231"}