Package 72843-576-01

Brand: olanzapine intramuscular

Generic: olanzapine
NDC Package

Package Facts

Identity

Package NDC 72843-576-01
Digits Only 7284357601
Product NDC 72843-576
Description

1 VIAL in 1 CARTON (72843-576-01) / 2 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2020-05-08
Brand olanzapine intramuscular
Generic olanzapine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR"], "spl_id": "38d62b8c-b92a-86fb-e063-6294a90a111d", "openfda": {"nui": ["N0000175430"], "upc": ["0072843576011"], "unii": ["N7U69T4SZR"], "rxcui": ["485968"], "spl_set_id": ["6a279fe1-ed99-4a62-b2c7-831961470fa9"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["UBI Pharma Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (72843-576-01)  / 2 mL in 1 VIAL", "package_ndc": "72843-576-01", "marketing_start_date": "20200508"}], "brand_name": "Olanzapine Intramuscular", "product_id": "72843-576_38d62b8c-b92a-86fb-e063-6294a90a111d", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "72843-576", "generic_name": "Olanzapine", "labeler_name": "UBI Pharma Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olanzapine", "brand_name_suffix": "Intramuscular", "active_ingredients": [{"name": "OLANZAPINE", "strength": "10 mg/2mL"}], "application_number": "ANDA211072", "marketing_category": "ANDA", "marketing_start_date": "20200508", "listing_expiration_date": "20261231"}