Package 63187-403-60

Brand: mirtazapine

Generic: mirtazapine
NDC Package

Package Facts

Identity

Package NDC 63187-403-60
Digits Only 6318740360
Product NDC 63187-403
Description

60 TABLET, FILM COATED in 1 BOTTLE (63187-403-60)

Marketing

Marketing Status
Marketed Since 2019-01-01
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": "1b0a2717-1fd5-46a0-9e7c-8368f21575cc", "openfda": {"unii": ["A051Q2099Q"], "rxcui": ["314111"], "spl_set_id": ["a96e0d95-1a7b-4588-923a-2169b5506203"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (63187-403-60)", "package_ndc": "63187-403-60", "marketing_start_date": "20190101"}], "brand_name": "Mirtazapine", "product_id": "63187-403_1b0a2717-1fd5-46a0-9e7c-8368f21575cc", "dosage_form": "TABLET, FILM COATED", "product_ndc": "63187-403", "generic_name": "Mirtazapine", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mirtazapine", "active_ingredients": [{"name": "MIRTAZAPINE", "strength": "30 mg/1"}], "application_number": "ANDA076921", "marketing_category": "ANDA", "marketing_start_date": "20090817", "listing_expiration_date": "20261231"}