Package 70518-0110-0

Brand: olanzapine

Generic: olanzapine
NDC Package

Package Facts

Identity

Package NDC 70518-0110-0
Digits Only 7051801100
Product NDC 70518-0110
Product ID 70518-0110_47e28597-136e-217d-e063-6294a90a2cec
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0110-0)

Marketing

Marketing Status
Marketed Since 2017-01-10
Brand olanzapine
Generic olanzapine
Sample Package No

Linked Drug Pages (0)

No linked drugs yet.

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "47e28597-136e-217d-e063-6294a90a2cec", "openfda": {"nui": ["N0000175430"], "unii": ["N7U69T4SZR"], "rxcui": ["312078"], "spl_set_id": ["dc56c264-d10e-4059-b0d5-2feff16b345d"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0110-0)", "package_ndc": "70518-0110-0", "marketing_start_date": "20170110"}], "brand_name": "Olanzapine", "product_id": "70518-0110_47e28597-136e-217d-e063-6294a90a2cec", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "70518-0110", "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": "20170110", "listing_expiration_date": "20271231"}