Package 0904-6519-61

Brand: mirtazapine

Generic: mirtazapine
NDC Package

Package Facts

Identity

Package NDC 0904-6519-61
Digits Only 0904651961
Product NDC 0904-6519
Product ID 0904-6519_2c3b820d-5318-42f7-b94e-2a70d659af71
Description

100 BLISTER PACK in 1 CARTON (0904-6519-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2007-08-22
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": "2c3b820d-5318-42f7-b94e-2a70d659af71", "openfda": {"unii": ["A051Q2099Q"], "rxcui": ["311725"], "spl_set_id": ["a80463be-f2d2-4074-9bd8-5e52b0832b3a"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-6519-61)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0904-6519-61", "marketing_start_date": "20070822"}], "brand_name": "Mirtazapine", "product_id": "0904-6519_2c3b820d-5318-42f7-b94e-2a70d659af71", "dosage_form": "TABLET, FILM COATED", "product_ndc": "0904-6519", "generic_name": "Mirtazapine", "labeler_name": "Major Pharmaceuticals", "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": "20070822", "listing_expiration_date": "20261231"}