Package 66993-608-04

Brand: mirtazapine

Generic: mirtazapine
NDC Package

Package Facts

Identity

Package NDC 66993-608-04
Digits Only 6699360804
Product NDC 66993-608
Description

500 TABLET, FILM COATED in 1 BOTTLE (66993-608-04)

Marketing

Marketing Status
Marketed Since 2023-09-01
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": "e1a19354-1c97-49ed-8ec9-bb895dbe69f3", "openfda": {"upc": ["0366993607306", "0366993607047", "0366993608044"], "unii": ["A051Q2099Q"], "rxcui": ["311725", "311726", "314111", "476809"], "spl_set_id": ["8b2a08f7-4803-42fa-a2b5-5ea51f8ef7e4"], "manufacturer_name": ["Prasco Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (66993-608-04)", "package_ndc": "66993-608-04", "marketing_start_date": "20230901"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (66993-608-30)", "package_ndc": "66993-608-30", "marketing_start_date": "20230901"}], "brand_name": "Mirtazapine", "product_id": "66993-608_e1a19354-1c97-49ed-8ec9-bb895dbe69f3", "dosage_form": "TABLET, FILM COATED", "product_ndc": "66993-608", "generic_name": "Mirtazapine", "labeler_name": "Prasco Laboratories", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mirtazapine", "active_ingredients": [{"name": "MIRTAZAPINE", "strength": "30 mg/1"}], "application_number": "ANDA216751", "marketing_category": "ANDA", "marketing_start_date": "20230901", "listing_expiration_date": "20261231"}