Package 70518-4322-0

Brand: mirtazapine

Generic: mirtazapine
NDC Package

Package Facts

Identity

Package NDC 70518-4322-0
Digits Only 7051843220
Product NDC 70518-4322
Product ID 70518-4322_402edcd0-e3d3-bf53-e063-6294a90a7076
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4322-0)

Marketing

Marketing Status
Marketed Since 2025-03-28
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": "402edcd0-e3d3-bf53-e063-6294a90a7076", "openfda": {"unii": ["A051Q2099Q"], "rxcui": ["311725"], "spl_set_id": ["412abf0e-1f96-4d4d-bb56-a23d4699b14c"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4322-0)", "package_ndc": "70518-4322-0", "marketing_start_date": "20250328"}], "brand_name": "Mirtazapine", "product_id": "70518-4322_402edcd0-e3d3-bf53-e063-6294a90a7076", "dosage_form": "TABLET, FILM COATED", "product_ndc": "70518-4322", "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": "ANDA076122", "marketing_category": "ANDA", "marketing_start_date": "20250328", "listing_expiration_date": "20261231"}