Package 51079-087-20

Brand: mirtazapine

Generic: mirtazapine
NDC Package

Package Facts

Identity

Package NDC 51079-087-20
Digits Only 5107908720
Product NDC 51079-087
Product ID 51079-087_3a87423c-fbbb-b2a4-e063-6394a90a0db3
Description

100 BLISTER PACK in 1 CARTON (51079-087-20) / 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-087-01)

Marketing

Marketing Status
Marketed Since 2003-08-01
Brand mirtazapine
Generic mirtazapine
Sample Package No

Linked Drug Pages (1)

Mirtazapine ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3a87423c-fbbb-b2a4-e063-6394a90a0db3", "openfda": {"unii": ["A051Q2099Q"], "rxcui": ["311725", "311726", "314111"], "spl_set_id": ["6837b69b-2f86-42cf-b48d-b4a3c7b5413f"], "manufacturer_name": ["Mylan Institutional Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (51079-087-20)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-087-01)", "package_ndc": "51079-087-20", "marketing_start_date": "20030801"}], "brand_name": "Mirtazapine", "product_id": "51079-087_3a87423c-fbbb-b2a4-e063-6394a90a0db3", "dosage_form": "TABLET, FILM COATED", "product_ndc": "51079-087", "generic_name": "Mirtazapine", "labeler_name": "Mylan Institutional Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mirtazapine", "active_ingredients": [{"name": "MIRTAZAPINE", "strength": "30 mg/1"}], "application_number": "ANDA076122", "marketing_category": "ANDA", "marketing_start_date": "20030801", "listing_expiration_date": "20261231"}