Package 60687-584-21

Brand: mirtazapine

Generic: mirtazapine
NDC Package

Package Facts

Identity

Package NDC 60687-584-21
Digits Only 6068758421
Product NDC 60687-584
Description

30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-584-21) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-584-11)

Marketing

Marketing Status
Marketed Since 2022-08-29
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": "2b24b256-28e5-28e1-e063-6294a90a8d89", "openfda": {"unii": ["A051Q2099Q"], "rxcui": ["476809"], "spl_set_id": ["3b7a5f44-8da6-4196-bb5d-8d2770af1b3a"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-584-21)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-584-11)", "package_ndc": "60687-584-21", "marketing_start_date": "20220829"}], "brand_name": "Mirtazapine", "product_id": "60687-584_2b24b256-28e5-28e1-e063-6294a90a8d89", "dosage_form": "TABLET, FILM COATED", "product_ndc": "60687-584", "generic_name": "Mirtazapine", "labeler_name": "American Health Packaging", "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": "20220829", "listing_expiration_date": "20261231"}