Package 68788-4012-3

Brand: olanzapine

Generic: olanzapine
NDC Package

Package Facts

Identity

Package NDC 68788-4012-3
Digits Only 6878840123
Product NDC 68788-4012
Product ID 68788-4012_cfc0f187-d3ff-4bbb-9129-0e94c6eda0ee
Description

30 TABLET, FILM COATED in 1 BOTTLE (68788-4012-3)

Marketing

Marketing Status
Marketed Since 2025-09-05
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": "cfc0f187-d3ff-4bbb-9129-0e94c6eda0ee", "openfda": {"nui": ["N0000175430"], "unii": ["N7U69T4SZR"], "rxcui": ["200034"], "spl_set_id": ["cfc0f187-d3ff-4bbb-9129-0e94c6eda0ee"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68788-4012-3)", "package_ndc": "68788-4012-3", "marketing_start_date": "20250905"}], "brand_name": "Olanzapine", "product_id": "68788-4012_cfc0f187-d3ff-4bbb-9129-0e94c6eda0ee", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "68788-4012", "generic_name": "Olanzapine", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olanzapine", "active_ingredients": [{"name": "OLANZAPINE", "strength": "2.5 mg/1"}], "application_number": "ANDA076255", "marketing_category": "ANDA", "marketing_start_date": "20250905", "listing_expiration_date": "20261231"}