Package 63629-9255-1

Brand: mirtazapine

Generic: mirtazapine
NDC Package

Package Facts

Identity

Package NDC 63629-9255-1
Digits Only 6362992551
Product NDC 63629-9255
Description

30 TABLET, FILM COATED in 1 BOTTLE (63629-9255-1)

Marketing

Marketing Status
Marketed Since 2022-04-12
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": "4680318e-0f8f-4048-a2fc-2da8c86abfab", "openfda": {"unii": ["A051Q2099Q"], "rxcui": ["476809"], "spl_set_id": ["bd532a25-cfde-4c7d-8015-ba40609fb95c"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (63629-9255-1)", "package_ndc": "63629-9255-1", "marketing_start_date": "20220412"}], "brand_name": "Mirtazapine", "product_id": "63629-9255_4680318e-0f8f-4048-a2fc-2da8c86abfab", "dosage_form": "TABLET, FILM COATED", "product_ndc": "63629-9255", "generic_name": "Mirtazapine", "labeler_name": "Bryant Ranch Prepack", "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"}