Package 0615-8244-39

Brand: olanzapine

Generic: olanzapine
NDC Package

Package Facts

Identity

Package NDC 0615-8244-39
Digits Only 0615824439
Product NDC 0615-8244
Product ID 0615-8244_23d2c50e-1be1-4357-bb2f-a9903ba4a43b
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8244-39)

Marketing

Marketing Status
Marketed Since 2018-11-02
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": "23d2c50e-1be1-4357-bb2f-a9903ba4a43b", "openfda": {"nui": ["N0000175430"], "unii": ["N7U69T4SZR"], "rxcui": ["200034", "283639", "312077", "312078", "314154"], "spl_set_id": ["87b7fb23-c9b7-433f-bd17-cd3e91714c27"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["NCS HealthCare of KY, LLC dba Vangard Labs"]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET, FILM COATED in 1 BLISTER PACK (0615-8244-05)", "package_ndc": "0615-8244-05", "marketing_start_date": "20240724"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8244-39)", "package_ndc": "0615-8244-39", "marketing_start_date": "20181102"}], "brand_name": "Olanzapine", "product_id": "0615-8244_23d2c50e-1be1-4357-bb2f-a9903ba4a43b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "0615-8244", "generic_name": "Olanzapine", "labeler_name": "NCS HealthCare of KY, LLC dba Vangard Labs", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olanzapine", "active_ingredients": [{"name": "OLANZAPINE", "strength": "5 mg/1"}], "application_number": "ANDA202862", "marketing_category": "ANDA", "marketing_start_date": "20140822", "listing_expiration_date": "20261231"}