Package 0121-1072-55

Brand: olanzapine intramuscular

Generic: olanzapine
NDC Package

Package Facts

Identity

Package NDC 0121-1072-55
Digits Only 0121107255
Product NDC 0121-1072
Description

1 VIAL in 1 CARTON (0121-1072-55) / 2 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2025-07-25
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": "1e5f9343-d43d-4ff7-b1ae-b6358640bbba", "openfda": {"nui": ["N0000175430"], "upc": ["0301211072559"], "unii": ["N7U69T4SZR"], "rxcui": ["485968"], "spl_set_id": ["9d9f25d5-4513-434a-a37a-392a0c978f2e"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["PAI Holdings, LLC dba PAI Pharma"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (0121-1072-55)  / 2 mL in 1 VIAL", "package_ndc": "0121-1072-55", "marketing_start_date": "20250725"}], "brand_name": "Olanzapine Intramuscular", "product_id": "0121-1072_1e5f9343-d43d-4ff7-b1ae-b6358640bbba", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "0121-1072", "generic_name": "Olanzapine", "labeler_name": "PAI Holdings, LLC dba PAI Pharma", "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": "20250725", "listing_expiration_date": "20261231"}