Package 70518-0921-0

Brand: olanzapine

Generic: olanzapine
NDC Package

Package Facts

Identity

Package NDC 70518-0921-0
Digits Only 7051809210
Product NDC 70518-0921
Product ID 70518-0921_4847a639-4ce1-ff9e-e063-6294a90a4fee
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0921-0)

Marketing

Marketing Status
Marketed Since 2017-12-26
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": "4847a639-4ce1-ff9e-e063-6294a90a4fee", "openfda": {"nui": ["N0000175430"], "unii": ["N7U69T4SZR"], "rxcui": ["314154"], "spl_set_id": ["88edb3fc-fcb6-4483-859d-f830b077aca2"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0921-0)", "package_ndc": "70518-0921-0", "marketing_start_date": "20171226"}], "brand_name": "Olanzapine", "product_id": "70518-0921_4847a639-4ce1-ff9e-e063-6294a90a4fee", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "70518-0921", "generic_name": "Olanzapine", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olanzapine", "active_ingredients": [{"name": "OLANZAPINE", "strength": "10 mg/1"}], "application_number": "ANDA202862", "marketing_category": "ANDA", "marketing_start_date": "20171226", "listing_expiration_date": "20271231"}