Package 70518-2453-0

Brand: mirtazapine

Generic: mirtazapine
NDC Package

Package Facts

Identity

Package NDC 70518-2453-0
Digits Only 7051824530
Product NDC 70518-2453
Product ID 70518-2453_4a28cf77-a03a-0bf2-e063-6394a90acb34
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2453-0)

Marketing

Marketing Status
Marketed Since 2019-11-25
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": "4a28cf77-a03a-0bf2-e063-6394a90acb34", "openfda": {"unii": ["A051Q2099Q"], "rxcui": ["311725"], "spl_set_id": ["f54718d1-3ef7-4472-9e97-90e5fd30db4d"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2453-0)", "package_ndc": "70518-2453-0", "marketing_start_date": "20191125"}], "brand_name": "Mirtazapine", "product_id": "70518-2453_4a28cf77-a03a-0bf2-e063-6394a90acb34", "dosage_form": "TABLET, FILM COATED", "product_ndc": "70518-2453", "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": "20191125", "listing_expiration_date": "20271231"}