Package 67184-0573-1

Brand: olanzapine

Generic: olanzapine
NDC Package

Package Facts

Identity

Package NDC 67184-0573-1
Digits Only 6718405731
Product NDC 67184-0573
Description

1 VIAL in 1 CARTON (67184-0573-1) / 2 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2025-11-11
Brand olanzapine
Generic olanzapine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR"], "spl_id": "816c3bbf-aa02-47e2-88d2-3a50c7764a84", "openfda": {"nui": ["N0000175430"], "unii": ["N7U69T4SZR"], "rxcui": ["485968"], "spl_set_id": ["12ce860a-6f22-4db6-8acf-786b40f5a5a5"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Qilu Pharmaceutical Co., Ltd."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (67184-0573-1)  / 2 mL in 1 VIAL", "package_ndc": "67184-0573-1", "marketing_start_date": "20251111"}], "brand_name": "Olanzapine", "product_id": "67184-0573_816c3bbf-aa02-47e2-88d2-3a50c7764a84", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "67184-0573", "generic_name": "Olanzapine", "labeler_name": "Qilu Pharmaceutical Co., Ltd.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olanzapine", "active_ingredients": [{"name": "OLANZAPINE", "strength": "10 mg/2mL"}], "application_number": "ANDA218116", "marketing_category": "ANDA", "marketing_start_date": "20251111", "listing_expiration_date": "20261231"}