Package 0143-9199-01

Brand: olanzapine

Generic: olanzapine
NDC Package

Package Facts

Identity

Package NDC 0143-9199-01
Digits Only 0143919901
Product NDC 0143-9199
Product ID 0143-9199_0143693c-5d42-4674-9b76-06e8e9e0ed63
Description

1 VIAL in 1 CARTON (0143-9199-01) / 2 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2025-09-18
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": ["INTRAMUSCULAR"], "spl_id": "0143693c-5d42-4674-9b76-06e8e9e0ed63", "openfda": {"nui": ["N0000175430"], "upc": ["0301439199014"], "unii": ["N7U69T4SZR"], "rxcui": ["485968"], "spl_set_id": ["63bcfe98-d1fc-4cd7-9212-f59ee4dcc6d1"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (0143-9199-01)  / 2 mL in 1 VIAL", "package_ndc": "0143-9199-01", "marketing_start_date": "20250918"}], "brand_name": "Olanzapine", "product_id": "0143-9199_0143693c-5d42-4674-9b76-06e8e9e0ed63", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "0143-9199", "generic_name": "Olanzapine", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "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": "20250918", "listing_expiration_date": "20261231"}