Package 68788-8459-6

Brand: mirtazapine

Generic: mirtazapine
NDC Package

Package Facts

Identity

Package NDC 68788-8459-6
Digits Only 6878884596
Product NDC 68788-8459
Description

60 TABLET, FILM COATED in 1 BOTTLE (68788-8459-6)

Marketing

Marketing Status
Marketed Since 2023-06-14
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": "36a45881-20c0-4364-b413-98d54eb1909f", "openfda": {"unii": ["A051Q2099Q"], "rxcui": ["311726"], "spl_set_id": ["2a0689ae-5650-42d1-ac9d-56dd2b467727"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68788-8459-3)", "package_ndc": "68788-8459-3", "marketing_start_date": "20230614"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68788-8459-6)", "package_ndc": "68788-8459-6", "marketing_start_date": "20230614"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68788-8459-9)", "package_ndc": "68788-8459-9", "marketing_start_date": "20230614"}], "brand_name": "Mirtazapine", "product_id": "68788-8459_36a45881-20c0-4364-b413-98d54eb1909f", "dosage_form": "TABLET, FILM COATED", "product_ndc": "68788-8459", "generic_name": "Mirtazapine", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mirtazapine", "active_ingredients": [{"name": "MIRTAZAPINE", "strength": "45 mg/1"}], "application_number": "ANDA076921", "marketing_category": "ANDA", "marketing_start_date": "20230614", "listing_expiration_date": "20261231"}