Package 60505-3112-0

Brand: olanzapine

Generic: olanzapine
NDC Package

Package Facts

Identity

Package NDC 60505-3112-0
Digits Only 6050531120
Product NDC 60505-3112
Product ID 60505-3112_2dd39227-59ef-df97-a57e-d5a013dc132f
Description

10 BLISTER PACK in 1 CARTON (60505-3112-0) / 10 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2012-04-23
Brand olanzapine
Generic olanzapine
Sample Package No

Linked Drug Pages (1)

Olanzapine ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2dd39227-59ef-df97-a57e-d5a013dc132f", "openfda": {"nui": ["N0000175430"], "upc": ["0360505311286", "0360505311187", "0360505311385", "0360505311484", "0360505314089", "0360505311088"], "unii": ["N7U69T4SZR"], "rxcui": ["200034", "283639", "312077", "312078", "312079", "314154"], "spl_set_id": ["3347d1c8-04c9-5ce1-8cda-b38e0412b709"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Apotex Corp."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 CARTON (60505-3112-0)  / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "60505-3112-0", "marketing_start_date": "20120423"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (60505-3112-8)", "package_ndc": "60505-3112-8", "marketing_start_date": "20120423"}], "brand_name": "Olanzapine", "product_id": "60505-3112_2dd39227-59ef-df97-a57e-d5a013dc132f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "60505-3112", "generic_name": "Olanzapine", "labeler_name": "Apotex Corp.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olanzapine", "active_ingredients": [{"name": "OLANZAPINE", "strength": "7.5 mg/1"}], "application_number": "ANDA090798", "marketing_category": "ANDA", "marketing_start_date": "20120423", "listing_expiration_date": "20271231"}