Package 72189-578-30

Brand: olanzapine

Generic: olanzapine
NDC Package

Package Facts

Identity

Package NDC 72189-578-30
Digits Only 7218957830
Product NDC 72189-578
Product ID 72189-578_22528ae1-e370-48e1-e063-6294a90a3dd2
Description

30 TABLET, FILM COATED in 1 BOTTLE (72189-578-30)

Marketing

Marketing Status
Marketed Since 2024-09-17
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": "22528ae1-e370-48e1-e063-6294a90a3dd2", "openfda": {"nui": ["N0000175430"], "unii": ["N7U69T4SZR"], "rxcui": ["312079"], "spl_set_id": ["22528ae1-e36f-48e1-e063-6294a90a3dd2"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72189-578-30)", "package_ndc": "72189-578-30", "marketing_start_date": "20240917"}], "brand_name": "Olanzapine", "product_id": "72189-578_22528ae1-e370-48e1-e063-6294a90a3dd2", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "72189-578", "generic_name": "Olanzapine", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olanzapine", "active_ingredients": [{"name": "OLANZAPINE", "strength": "7.5 mg/1"}], "application_number": "ANDA202862", "marketing_category": "ANDA", "marketing_start_date": "20240917", "listing_expiration_date": "20261231"}