Package 63629-8718-1

Brand: olanzapine

Generic: olanzapine
NDC Package

Package Facts

Identity

Package NDC 63629-8718-1
Digits Only 6362987181
Product NDC 63629-8718
Product ID 63629-8718_3364e551-5f70-d3ba-e063-6394a90afbe1
Description

30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (63629-8718-1)

Marketing

Marketing Status
Marketed Since 2011-10-24
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": "3364e551-5f70-d3ba-e063-6394a90afbe1", "openfda": {"nui": ["N0000175430"], "unii": ["N7U69T4SZR"], "rxcui": ["312076"], "spl_set_id": ["ed93d6b9-912a-444a-a695-439d0bfb877a"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (63629-8718-1)", "package_ndc": "63629-8718-1", "marketing_start_date": "20111024"}], "brand_name": "Olanzapine", "product_id": "63629-8718_3364e551-5f70-d3ba-e063-6394a90afbe1", "dosage_form": "TABLET, ORALLY DISINTEGRATING", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "63629-8718", "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": "ANDA091265", "marketing_category": "ANDA", "marketing_start_date": "20111024", "listing_expiration_date": "20261231"}