Package 50090-2800-0

Brand: mirtazapine

Generic: mirtazapine
NDC Package

Package Facts

Identity

Package NDC 50090-2800-0
Digits Only 5009028000
Product NDC 50090-2800
Product ID 50090-2800_1227fedd-ff4c-4393-aa32-73ad0b8424b4
Description

30 TABLET, FILM COATED in 1 BOTTLE (50090-2800-0)

Marketing

Marketing Status
Marketed Since 2017-03-02
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": "1227fedd-ff4c-4393-aa32-73ad0b8424b4", "openfda": {"unii": ["A051Q2099Q"], "rxcui": ["311725", "314111"], "spl_set_id": ["552e2261-53db-4a27-b277-f7b62c3ea2ed"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-2800-0)", "package_ndc": "50090-2800-0", "marketing_start_date": "20170302"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-2800-1)", "package_ndc": "50090-2800-1", "marketing_start_date": "20170119"}], "brand_name": "Mirtazapine", "product_id": "50090-2800_1227fedd-ff4c-4393-aa32-73ad0b8424b4", "dosage_form": "TABLET, FILM COATED", "product_ndc": "50090-2800", "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": "20041022", "listing_expiration_date": "20271231"}