Package 71335-2412-1

Brand: mirtazapine

Generic: mirtazapine
NDC Package

Package Facts

Identity

Package NDC 71335-2412-1
Digits Only 7133524121
Product NDC 71335-2412
Product ID 71335-2412_661491d5-5639-41ba-a627-8fc3d3ed1c0a
Description

30 TABLET, FILM COATED in 1 BOTTLE (71335-2412-1)

Marketing

Marketing Status
Marketed Since 2024-06-10
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": "661491d5-5639-41ba-a627-8fc3d3ed1c0a", "openfda": {"unii": ["A051Q2099Q"], "rxcui": ["476809"], "spl_set_id": ["6b6e946c-54b5-40e3-918f-9cc29f04cd9a"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-2412-1)", "package_ndc": "71335-2412-1", "marketing_start_date": "20240610"}], "brand_name": "Mirtazapine", "product_id": "71335-2412_661491d5-5639-41ba-a627-8fc3d3ed1c0a", "dosage_form": "TABLET, FILM COATED", "product_ndc": "71335-2412", "generic_name": "Mirtazapine", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mirtazapine", "active_ingredients": [{"name": "MIRTAZAPINE", "strength": "7.5 mg/1"}], "application_number": "ANDA076921", "marketing_category": "ANDA", "marketing_start_date": "20041022", "listing_expiration_date": "20271231"}