Package 70518-0935-0

Brand: olanzapine

Generic: olanzapine
NDC Package

Package Facts

Identity

Package NDC 70518-0935-0
Digits Only 7051809350
Product NDC 70518-0935
Product ID 70518-0935_4847cdb9-db33-79ee-e063-6394a90acd9c
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0935-0)

Marketing

Marketing Status
Marketed Since 2018-01-05
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": "4847cdb9-db33-79ee-e063-6394a90acd9c", "openfda": {"nui": ["N0000175430"], "unii": ["N7U69T4SZR"], "rxcui": ["312078"], "spl_set_id": ["8e5ef52d-315b-4055-9e52-403e6f896f24"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0935-0)", "package_ndc": "70518-0935-0", "marketing_start_date": "20180105"}], "brand_name": "Olanzapine", "product_id": "70518-0935_4847cdb9-db33-79ee-e063-6394a90acd9c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "70518-0935", "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": "ANDA202862", "marketing_category": "ANDA", "marketing_start_date": "20180105", "listing_expiration_date": "20271231"}