Package 67046-1604-3

Brand: olanzapine

Generic: olanzapine
NDC Package

Package Facts

Identity

Package NDC 67046-1604-3
Digits Only 6704616043
Product NDC 67046-1604
Description

30 TABLET in 1 BLISTER PACK (67046-1604-3)

Marketing

Marketing Status
Marketed Since 2025-10-01
Brand olanzapine
Generic olanzapine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "40189aed-2898-e791-e063-6394a90a44f6", "openfda": {"nui": ["N0000175430"], "unii": ["N7U69T4SZR"], "rxcui": ["283639"], "spl_set_id": ["40187874-447a-de20-e063-6394a90aafe7"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (67046-1604-3)", "package_ndc": "67046-1604-3", "marketing_start_date": "20251001"}], "brand_name": "Olanzapine", "product_id": "67046-1604_40189aed-2898-e791-e063-6394a90a44f6", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "67046-1604", "generic_name": "Olanzapine", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olanzapine", "active_ingredients": [{"name": "OLANZAPINE", "strength": "20 mg/1"}], "application_number": "ANDA210022", "marketing_category": "ANDA", "marketing_start_date": "20251001", "listing_expiration_date": "20261231"}