Package 70518-1397-1

Brand: mirtazapine

Generic: mirtazapine
NDC Package

Package Facts

Identity

Package NDC 70518-1397-1
Digits Only 7051813971
Product NDC 70518-1397
Product ID 70518-1397_48fba7b0-90d0-f973-e063-6394a90a9672
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1397-1)

Marketing

Marketing Status
Marketed Since 2025-08-23
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": "48fba7b0-90d0-f973-e063-6394a90a9672", "openfda": {"unii": ["A051Q2099Q"], "rxcui": ["311725"], "spl_set_id": ["9135e7db-cba4-4150-a69c-fdf2a347a785"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1397-0)", "package_ndc": "70518-1397-0", "marketing_start_date": "20180831"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1397-1)", "package_ndc": "70518-1397-1", "marketing_start_date": "20250823"}], "brand_name": "Mirtazapine", "product_id": "70518-1397_48fba7b0-90d0-f973-e063-6394a90a9672", "dosage_form": "TABLET, FILM COATED", "product_ndc": "70518-1397", "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": "20180831", "listing_expiration_date": "20271231"}