Package 70518-0314-1

Brand: olanzapine

Generic: olanzapine
NDC Package

Package Facts

Identity

Package NDC 70518-0314-1
Digits Only 7051803141
Product NDC 70518-0314
Product ID 70518-0314_47e6f4fa-85ee-de93-e063-6394a90a429c
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0314-1)

Marketing

Marketing Status
Marketed Since 2022-06-10
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": "47e6f4fa-85ee-de93-e063-6394a90a429c", "openfda": {"nui": ["N0000175430"], "unii": ["N7U69T4SZR"], "rxcui": ["312078"], "spl_set_id": ["e830f488-c689-40f6-9351-f9c7454ff1ea"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0314-1)", "package_ndc": "70518-0314-1", "marketing_start_date": "20220610"}], "brand_name": "Olanzapine", "product_id": "70518-0314_47e6f4fa-85ee-de93-e063-6394a90a429c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "70518-0314", "generic_name": "Olanzapine", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olanzapine", "active_ingredients": [{"name": "OLANZAPINE", "strength": "5 mg/1"}], "application_number": "ANDA090798", "marketing_category": "ANDA", "marketing_start_date": "20170314", "listing_expiration_date": "20271231"}