Package 70518-0316-0

Brand: mirtazapine

Generic: mirtazapine
NDC Package

Package Facts

Identity

Package NDC 70518-0316-0
Digits Only 7051803160
Product NDC 70518-0316
Product ID 70518-0316_47e70afa-0f2e-ec9d-e063-6394a90a473f
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0316-0)

Marketing

Marketing Status
Marketed Since 2017-03-14
Brand mirtazapine
Generic mirtazapine
Sample Package No

Linked Drug Pages (0)

No linked drugs yet.

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "47e70afa-0f2e-ec9d-e063-6394a90a473f", "openfda": {"unii": ["A051Q2099Q"], "rxcui": ["314111"], "spl_set_id": ["eaef7ee6-7e23-4cc8-844c-a16ff7a732db"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0316-0)", "package_ndc": "70518-0316-0", "marketing_start_date": "20170314"}], "brand_name": "Mirtazapine", "product_id": "70518-0316_47e70afa-0f2e-ec9d-e063-6394a90a473f", "dosage_form": "TABLET, FILM COATED", "product_ndc": "70518-0316", "generic_name": "Mirtazapine", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mirtazapine", "active_ingredients": [{"name": "MIRTAZAPINE", "strength": "30 mg/1"}], "application_number": "ANDA076921", "marketing_category": "ANDA", "marketing_start_date": "20170314", "listing_expiration_date": "20271231"}