Package 70518-0180-0

Brand: mirtazapine

Generic: mirtazapine
NDC Package

Package Facts

Identity

Package NDC 70518-0180-0
Digits Only 7051801800
Product NDC 70518-0180
Product ID 70518-0180_47e46668-d67d-0d37-e063-6394a90a7dc4
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0180-0)

Marketing

Marketing Status
Marketed Since 2017-01-26
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": "47e46668-d67d-0d37-e063-6394a90a7dc4", "openfda": {"unii": ["A051Q2099Q"], "rxcui": ["311725"], "spl_set_id": ["d1b59d87-8442-4c15-8bb9-e39b198d8677"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0180-0)", "package_ndc": "70518-0180-0", "marketing_start_date": "20170126"}], "brand_name": "Mirtazapine", "product_id": "70518-0180_47e46668-d67d-0d37-e063-6394a90a7dc4", "dosage_form": "TABLET, FILM COATED", "product_ndc": "70518-0180", "generic_name": "Mirtazapine", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mirtazapine", "active_ingredients": [{"name": "MIRTAZAPINE", "strength": "15 mg/1"}], "application_number": "ANDA076921", "marketing_category": "ANDA", "marketing_start_date": "20170126", "listing_expiration_date": "20271231"}