Package 82804-067-30

Brand: olanzapine

Generic: olanzapine
NDC Package

Package Facts

Identity

Package NDC 82804-067-30
Digits Only 8280406730
Product NDC 82804-067
Description

30 TABLET, FILM COATED in 1 BOTTLE (82804-067-30)

Marketing

Marketing Status
Marketed Since 2024-01-31
Brand olanzapine
Generic olanzapine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "024e8e9b-a4fc-4882-b080-c070467166a6", "openfda": {"nui": ["N0000175430"], "upc": ["0382804067305"], "unii": ["N7U69T4SZR"], "rxcui": ["283639"], "spl_set_id": ["024e8e9b-a4fc-4882-b080-c070467166a6"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (82804-067-30)", "package_ndc": "82804-067-30", "marketing_start_date": "20240131"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (82804-067-60)", "package_ndc": "82804-067-60", "marketing_start_date": "20240131"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (82804-067-90)", "package_ndc": "82804-067-90", "marketing_start_date": "20240131"}], "brand_name": "Olanzapine", "product_id": "82804-067_024e8e9b-a4fc-4882-b080-c070467166a6", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "82804-067", "generic_name": "Olanzapine", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olanzapine", "active_ingredients": [{"name": "OLANZAPINE", "strength": "20 mg/1"}], "application_number": "ANDA090798", "marketing_category": "ANDA", "marketing_start_date": "20120423", "listing_expiration_date": "20261231"}