Package 70518-1838-0

Brand: mirtazapine

Generic: mirtazapine
NDC Package

Package Facts

Identity

Package NDC 70518-1838-0
Digits Only 7051818380
Product NDC 70518-1838
Product ID 70518-1838_497738f0-9d95-b22e-e063-6394a90a5d89
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1838-0)

Marketing

Marketing Status
Marketed Since 2019-01-30
Brand mirtazapine
Generic mirtazapine
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "497738f0-9d95-b22e-e063-6394a90a5d89", "openfda": {"unii": ["A051Q2099Q"], "rxcui": ["311725"], "spl_set_id": ["81d9e47e-ae81-4755-a5ee-546a038fadb4"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1838-0)", "package_ndc": "70518-1838-0", "marketing_start_date": "20190130"}], "brand_name": "Mirtazapine", "product_id": "70518-1838_497738f0-9d95-b22e-e063-6394a90a5d89", "dosage_form": "TABLET, FILM COATED", "product_ndc": "70518-1838", "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": "20190130", "listing_expiration_date": "20271231"}