Package 0781-9105-72

Brand: olanzapine

Generic: olanzapine
NDC Package

Package Facts

Identity

Package NDC 0781-9105-72
Digits Only 0781910572
Product NDC 0781-9105
Product ID 0781-9105_27a10706-f06f-407c-ae22-9a49d6a543e8
Description

1 VIAL in 1 CARTON (0781-9105-72) / 2 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2011-10-24
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": "27a10706-f06f-407c-ae22-9a49d6a543e8", "openfda": {"nui": ["N0000175430"], "unii": ["N7U69T4SZR"], "rxcui": ["485968"], "spl_set_id": ["c44a96cc-817d-4eb5-a13a-00977f76e666"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (0781-9105-72)  / 2 mL in 1 VIAL", "package_ndc": "0781-9105-72", "marketing_start_date": "20111024"}], "brand_name": "Olanzapine", "product_id": "0781-9105_27a10706-f06f-407c-ae22-9a49d6a543e8", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "0781-9105", "generic_name": "Olanzapine", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olanzapine", "active_ingredients": [{"name": "OLANZAPINE", "strength": "10 mg/2mL"}], "application_number": "ANDA201588", "marketing_category": "ANDA", "marketing_start_date": "20111024", "listing_expiration_date": "20261231"}