Package 67046-1590-3

Brand: mirtazapine

Generic: mirtazapine
NDC Package

Package Facts

Identity

Package NDC 67046-1590-3
Digits Only 6704615903
Product NDC 67046-1590
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1590-3)

Marketing

Marketing Status
Marketed Since 2025-09-16
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": "3eed81ad-e8ac-db55-e063-6394a90a054c", "openfda": {"unii": ["A051Q2099Q"], "rxcui": ["311725"], "spl_set_id": ["3eed8213-a240-fc4b-e063-6294a90a3b05"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1590-3)", "package_ndc": "67046-1590-3", "marketing_start_date": "20250916"}], "brand_name": "Mirtazapine", "product_id": "67046-1590_3eed81ad-e8ac-db55-e063-6394a90a054c", "dosage_form": "TABLET, FILM COATED", "product_ndc": "67046-1590", "generic_name": "Mirtazapine", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mirtazapine", "active_ingredients": [{"name": "MIRTAZAPINE", "strength": "15 mg/1"}], "application_number": "ANDA077666", "marketing_category": "ANDA", "marketing_start_date": "20250916", "listing_expiration_date": "20261231"}