Package 67046-1550-3

Brand: olanzapine

Generic: olanzapine
NDC Package

Package Facts

Identity

Package NDC 67046-1550-3
Digits Only 6704615503
Product NDC 67046-1550
Product ID 67046-1550_325d7012-77bd-83af-e063-6294a90a52ef
Description

30 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (67046-1550-3)

Marketing

Marketing Status
Marketed Since 2025-04-09
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": "325d7012-77bd-83af-e063-6294a90a52ef", "openfda": {"nui": ["N0000175430"], "unii": ["N7U69T4SZR"], "rxcui": ["314155"], "spl_set_id": ["325d5d69-5133-79ea-e063-6294a90afdd0"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (67046-1550-3)", "package_ndc": "67046-1550-3", "marketing_start_date": "20250409"}], "brand_name": "Olanzapine", "product_id": "67046-1550_325d7012-77bd-83af-e063-6294a90a52ef", "dosage_form": "TABLET, ORALLY DISINTEGRATING", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "67046-1550", "generic_name": "Olanzapine", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olanzapine", "active_ingredients": [{"name": "OLANZAPINE", "strength": "5 mg/1"}], "application_number": "ANDA091265", "marketing_category": "ANDA", "marketing_start_date": "20250409", "listing_expiration_date": "20261231"}