Package 72789-460-14

Brand: olanzapine

Generic: olanzapine
NDC Package

Package Facts

Identity

Package NDC 72789-460-14
Digits Only 7278946014
Product NDC 72789-460
Product ID 72789-460_3840298a-c3c2-01b5-e063-6394a90a0a60
Description

14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-460-14)

Marketing

Marketing Status
Marketed Since 2024-12-20
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": "3840298a-c3c2-01b5-e063-6394a90a0a60", "openfda": {"nui": ["N0000175430"], "upc": ["0372789460147"], "unii": ["N7U69T4SZR"], "rxcui": ["312078"], "spl_set_id": ["10043041-a632-4e57-bc08-37216dea8546"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-460-14)", "package_ndc": "72789-460-14", "marketing_start_date": "20241220"}], "brand_name": "Olanzapine", "product_id": "72789-460_3840298a-c3c2-01b5-e063-6394a90a0a60", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "72789-460", "generic_name": "Olanzapine", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olanzapine", "active_ingredients": [{"name": "OLANZAPINE", "strength": "5 mg/1"}], "application_number": "ANDA076255", "marketing_category": "ANDA", "marketing_start_date": "20131210", "listing_expiration_date": "20261231"}