Package 57664-510-83

Brand: mirtazapine

Generic: mirtazapine
NDC Package

Package Facts

Identity

Package NDC 57664-510-83
Digits Only 5766451083
Product NDC 57664-510
Product ID 57664-510_f5e842da-4922-4f1d-b2e0-a4c0be71e2a6
Description

30 TABLET in 1 BOTTLE (57664-510-83)

Marketing

Marketing Status
Marketed Since 2004-04-22
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": "f5e842da-4922-4f1d-b2e0-a4c0be71e2a6", "openfda": {"upc": ["0357664500835"], "unii": ["A051Q2099Q"], "rxcui": ["311725", "311726", "314111", "476809"], "spl_set_id": ["f23631be-c7ae-46e9-b771-a70be17bc9f0"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (57664-510-83)", "package_ndc": "57664-510-83", "marketing_start_date": "20040422"}], "brand_name": "Mirtazapine", "product_id": "57664-510_f5e842da-4922-4f1d-b2e0-a4c0be71e2a6", "dosage_form": "TABLET", "product_ndc": "57664-510", "generic_name": "Mirtazapine", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mirtazapine", "active_ingredients": [{"name": "MIRTAZAPINE", "strength": "7.5 mg/1"}], "application_number": "ANDA076541", "marketing_category": "ANDA", "marketing_start_date": "20040422", "listing_expiration_date": "20261231"}