Package 61919-153-60

Brand: mirtazapine

Generic: mirtazapine
NDC Package

Package Facts

Identity

Package NDC 61919-153-60
Digits Only 6191915360
Product NDC 61919-153
Product ID 61919-153_47e14699-4104-6433-e063-6394a90acbcc
Description

60 TABLET, FILM COATED in 1 BOTTLE (61919-153-60)

Marketing

Marketing Status
Marketed Since 2022-05-10
Brand mirtazapine
Generic mirtazapine
Sample Package No

Linked Drug Pages (1)

Mirtazapine ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "47e14699-4104-6433-e063-6394a90acbcc", "openfda": {"unii": ["A051Q2099Q"], "rxcui": ["311725"], "spl_set_id": ["dea8c09a-b759-1da7-e053-2a95a90a3346"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (61919-153-60)", "package_ndc": "61919-153-60", "marketing_start_date": "20220510"}], "brand_name": "Mirtazapine", "product_id": "61919-153_47e14699-4104-6433-e063-6394a90acbcc", "dosage_form": "TABLET, FILM COATED", "product_ndc": "61919-153", "generic_name": "Mirtazapine", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mirtazapine", "active_ingredients": [{"name": "MIRTAZAPINE", "strength": "15 mg/1"}], "application_number": "ANDA077666", "marketing_category": "ANDA", "marketing_start_date": "20220510", "listing_expiration_date": "20271231"}