Package 0615-8489-05
Brand: mirtazapine
Generic: mirtazapinePackage Facts
Identity
Package NDC
0615-8489-05
Digits Only
0615848905
Product NDC
0615-8489
Description
15 TABLET, FILM COATED in 1 BLISTER PACK (0615-8489-05)
Marketing
Marketing Status
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": "638be761-770a-4310-9296-00aa4a184425", "openfda": {"unii": ["A051Q2099Q"], "rxcui": ["476809"], "spl_set_id": ["70439462-b632-4d21-8067-560162db3137"], "manufacturer_name": ["NCS HealthCare of KY, LLC dba Vangard Labs"]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET, FILM COATED in 1 BLISTER PACK (0615-8489-05)", "package_ndc": "0615-8489-05", "marketing_start_date": "20230915"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8489-39)", "package_ndc": "0615-8489-39", "marketing_start_date": "20230915"}], "brand_name": "Mirtazapine", "product_id": "0615-8489_638be761-770a-4310-9296-00aa4a184425", "dosage_form": "TABLET, FILM COATED", "product_ndc": "0615-8489", "generic_name": "Mirtazapine", "labeler_name": "NCS HealthCare of KY, LLC dba Vangard Labs", "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": "20041022", "listing_expiration_date": "20261231"}