Package 72789-341-90

Brand: olanzapine

Generic: olanzapine
NDC Package

Package Facts

Identity

Package NDC 72789-341-90
Digits Only 7278934190
Product NDC 72789-341
Product ID 72789-341_31f578dc-776c-d6fa-e063-6394a90a0b26
Description

90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-341-90)

Marketing

Marketing Status
Marketed Since 2023-08-01
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": ["ORAL"], "spl_id": "31f578dc-776c-d6fa-e063-6394a90a0b26", "openfda": {"nui": ["N0000175430"], "upc": ["0372789341903"], "unii": ["N7U69T4SZR"], "rxcui": ["283639"], "spl_set_id": ["b6f0b2e2-3cbd-4564-8b3e-f811589af275"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-341-90)", "package_ndc": "72789-341-90", "marketing_start_date": "20230801"}], "brand_name": "Olanzapine", "product_id": "72789-341_31f578dc-776c-d6fa-e063-6394a90a0b26", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "72789-341", "generic_name": "Olanzapine", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olanzapine", "active_ingredients": [{"name": "OLANZAPINE", "strength": "20 mg/1"}], "application_number": "ANDA202862", "marketing_category": "ANDA", "marketing_start_date": "20140822", "listing_expiration_date": "20261231"}