Package 67046-1583-3

Brand: olanzapine

Generic: olanzapine
NDC Package

Package Facts

Identity

Package NDC 67046-1583-3
Digits Only 6704615833
Product NDC 67046-1583
Description

30 TABLET in 1 BLISTER PACK (67046-1583-3)

Marketing

Marketing Status
Marketed Since 2025-09-15
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": "3ed7888b-d94b-61e3-e063-6394a90a1de4", "openfda": {"nui": ["N0000175430"], "unii": ["N7U69T4SZR"], "rxcui": ["314154"], "spl_set_id": ["3ed78a7d-4014-d280-e063-6294a90a8ee9"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (67046-1583-3)", "package_ndc": "67046-1583-3", "marketing_start_date": "20250915"}], "brand_name": "Olanzapine", "product_id": "67046-1583_3ed7888b-d94b-61e3-e063-6394a90a1de4", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "67046-1583", "generic_name": "Olanzapine", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olanzapine", "active_ingredients": [{"name": "OLANZAPINE", "strength": "10 mg/1"}], "application_number": "ANDA210022", "marketing_category": "ANDA", "marketing_start_date": "20250915", "listing_expiration_date": "20261231"}