Package 72162-2368-0

Brand: olanzapine

Generic: olanzapine
NDC Package

Package Facts

Identity

Package NDC 72162-2368-0
Digits Only 7216223680
Product NDC 72162-2368
Product ID 72162-2368_66bc8218-ea99-4c2d-931d-c12a53fd33b8
Description

1000 TABLET, FILM COATED in 1 BOTTLE (72162-2368-0)

Marketing

Marketing Status
Marketed Since 2024-07-16
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": "66bc8218-ea99-4c2d-931d-c12a53fd33b8", "openfda": {"nui": ["N0000175430"], "unii": ["N7U69T4SZR"], "rxcui": ["314154"], "spl_set_id": ["f6fd7ceb-1457-4c3e-9d30-4f658f39d37d"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (72162-2368-0)", "package_ndc": "72162-2368-0", "marketing_start_date": "20240716"}], "brand_name": "Olanzapine", "product_id": "72162-2368_66bc8218-ea99-4c2d-931d-c12a53fd33b8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "72162-2368", "generic_name": "Olanzapine", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olanzapine", "active_ingredients": [{"name": "OLANZAPINE", "strength": "10 mg/1"}], "application_number": "ANDA202862", "marketing_category": "ANDA", "marketing_start_date": "20140822", "listing_expiration_date": "20261231"}