Package 70518-1764-0

Brand: olanzapine

Generic: olanzapine
NDC Package

Package Facts

Identity

Package NDC 70518-1764-0
Digits Only 7051817640
Product NDC 70518-1764
Product ID 70518-1764_4974003a-4507-1afb-e063-6394a90ae2d6
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1764-0)

Marketing

Marketing Status
Marketed Since 2019-01-02
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": "4974003a-4507-1afb-e063-6394a90ae2d6", "openfda": {"nui": ["N0000175430"], "unii": ["N7U69T4SZR"], "rxcui": ["312078"], "spl_set_id": ["3d69af75-7615-4ec2-b7ef-467b2558c5c8"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1764-0)", "package_ndc": "70518-1764-0", "marketing_start_date": "20190102"}], "brand_name": "Olanzapine", "product_id": "70518-1764_4974003a-4507-1afb-e063-6394a90ae2d6", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "70518-1764", "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": "ANDA076255", "marketing_category": "ANDA", "marketing_start_date": "20190102", "listing_expiration_date": "20271231"}