Package 71335-3038-1

Brand: mirtazapine

Generic: mirtazapine
NDC Package

Package Facts

Identity

Package NDC 71335-3038-1
Digits Only 7133530381
Product NDC 71335-3038
Description

30 TABLET, FILM COATED in 1 BOTTLE (71335-3038-1)

Marketing

Marketing Status
Marketed Since 2025-12-03
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": "0c65a448-a721-41b5-9545-a5e90b83cda3", "openfda": {"unii": ["A051Q2099Q"], "rxcui": ["476809"], "spl_set_id": ["c2b38cc5-7738-44fa-9bef-89a18a1039b2"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-3038-1)", "package_ndc": "71335-3038-1", "marketing_start_date": "20251203"}], "brand_name": "Mirtazapine", "product_id": "71335-3038_0c65a448-a721-41b5-9545-a5e90b83cda3", "dosage_form": "TABLET, FILM COATED", "product_ndc": "71335-3038", "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": "20090817", "listing_expiration_date": "20261231"}