Package 70518-2819-2

Brand: mirtazapine

Generic: mirtazapine
NDC Package

Package Facts

Identity

Package NDC 70518-2819-2
Digits Only 7051828192
Product NDC 70518-2819
Product ID 70518-2819_4ab63e12-0986-52a7-e063-6294a90a549c
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2819-2)

Marketing

Marketing Status
Marketed Since 2023-07-12
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": "4ab63e12-0986-52a7-e063-6294a90a549c", "openfda": {"unii": ["A051Q2099Q"], "rxcui": ["476809"], "spl_set_id": ["10ea9d83-19c3-4f3b-a1cc-cfc48b42507f"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2819-2)", "package_ndc": "70518-2819-2", "marketing_start_date": "20230712"}], "brand_name": "Mirtazapine", "product_id": "70518-2819_4ab63e12-0986-52a7-e063-6294a90a549c", "dosage_form": "TABLET, FILM COATED", "product_ndc": "70518-2819", "generic_name": "Mirtazapine", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mirtazapine", "active_ingredients": [{"name": "MIRTAZAPINE", "strength": "7.5 mg/1"}], "application_number": "ANDA076921", "marketing_category": "ANDA", "marketing_start_date": "20200723", "listing_expiration_date": "20271231"}