Package 71335-2963-1

Brand: mirtazapine

Generic: mirtazapine
NDC Package

Package Facts

Identity

Package NDC 71335-2963-1
Digits Only 7133529631
Product NDC 71335-2963
Description

500 TABLET in 1 BOTTLE (71335-2963-1)

Marketing

Marketing Status
Marketed Since 2025-10-29
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": "4252f585-b169-a518-e063-6394a90a04b6", "openfda": {"unii": ["A051Q2099Q"], "rxcui": ["314111"], "spl_set_id": ["356eb045-6347-49cc-818e-65b1cdff8f4e"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (71335-2963-1)", "package_ndc": "71335-2963-1", "marketing_start_date": "20251029"}], "brand_name": "Mirtazapine", "product_id": "71335-2963_4252f585-b169-a518-e063-6394a90a04b6", "dosage_form": "TABLET", "product_ndc": "71335-2963", "generic_name": "Mirtazapine", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mirtazapine", "active_ingredients": [{"name": "MIRTAZAPINE", "strength": "30 mg/1"}], "application_number": "ANDA076541", "marketing_category": "ANDA", "marketing_start_date": "20040422", "listing_expiration_date": "20261231"}