Package 68071-4989-3
Brand: mirtazapine
Generic: mirtazapinePackage 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
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"}