Package 68071-4989-3

Brand: mirtazapine

Generic: mirtazapine
NDC Package

Package Facts

Identity

Package NDC 68071-4989-3
Digits Only 6807149893
Product NDC 68071-4989
Description

30 TABLET, FILM COATED in 1 BOTTLE (68071-4989-3)

Marketing

Marketing Status
Marketed Since 2019-07-25
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": "1b305c50-b2f3-6e01-e063-6394a90a0ce1", "openfda": {"upc": ["0368071498936"], "unii": ["A051Q2099Q"], "rxcui": ["314111"], "spl_set_id": ["8e839bb2-2f67-f224-e053-2a95a90ae5d8"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68071-4989-3)", "package_ndc": "68071-4989-3", "marketing_start_date": "20190725"}], "brand_name": "Mirtazapine", "product_id": "68071-4989_1b305c50-b2f3-6e01-e063-6394a90a0ce1", "dosage_form": "TABLET, FILM COATED", "product_ndc": "68071-4989", "generic_name": "Mirtazapine", "labeler_name": "NuCare Pharmaceuticals,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": "20041022", "listing_expiration_date": "20261231"}